CausalSentinel

Protein Dossier — LYVE1 (Lymphatic vessel endothelial hyaluronic acid receptor 1)

MR feasibility tier: A — Published pQTL-MR estimates exist for this protein (retrieved below - not computed here).

1. Published MR estimates (retrieved, not computed)

Outcome beta se p method nSNP cis/trans coloc
Diagnoses - main ICD10: N40 Hyperplasia of prostate 0.488 0.105 3.63e-06 Wald ratio 1 cis NA
Hippocampus volume 77.7 30.5 0.011 Wald ratio 1 cis NA
Non-cancer illness code self-reported: uterine fibroids 0.251 0.104 0.0155 Wald ratio 1 cis NA
Height 0.0542 0.0233 0.02 Wald ratio 1 cis NA
Non-cancer illness code self-reported: iron deficiency anaemia 0.368 0.159 0.0208 Wald ratio 1 cis NA
Diagnoses - main ICD10: I83 Varicose veins of lower extremities 0.209 0.0932 0.0248 Wald ratio 1 cis NA
Non-cancer illness code self-reported: bladder problem (not cancer) 0.338 0.157 0.0311 Wald ratio 1 cis NA
Forearm bone mineral density -0.217 0.107 0.0423 Wald ratio 1 cis NA
HbA1C -0.0607 0.0309 0.0494 Wald ratio 1 cis NA
Birth weight -0.0485 0.0252 0.0543 Wald ratio 1 cis NA
Primary sclerosing cholangitis -0.388 0.209 0.0629 Wald ratio 1 cis NA
Cough on most days 0.136 0.0735 0.0634 Wald ratio 1 cis NA
…and 64 more outcomes (see JSON)              

2. pQTL instrument availability (Tier-B probe)

Dataset Trait Author Year
prot-c-3206_4_2 LYVE1 Suhre K 2019

3. GWAS Catalog results — traits with signal at this locus

18 association rows across 16 traits (9 genome-wide significant rows). Associations are loci, not causal claims; the mapped gene at a locus is not necessarily the effector gene.

Trait best p lead SNP n assoc study MR status
LYVE1 protein levels 8e-88 rs114708736 3 GCST90469832 no MR -> candidate analysis
Serum levels of protein LYVE1 1e-19 rs116573529 1 GCST90088269 no MR -> candidate analysis
Lymphatic vessel endothelial hyaluronic acid receptor 1 leve 7e-12 rs11042892 1 GCST90248369 no MR -> candidate analysis
Blood protein levels 3e-11 rs114527818 1 GCST006585 no MR -> candidate analysis
Forced expiratory volume in 1 second (FEV1) 5e-11 rs7115735 1 GCST90705070 no MR -> candidate analysis
Peak expiratory flow 2e-9 rs7115735 1 GCST90244095 no MR -> candidate analysis
White blood cell count (monocyte) 3e-8 rs76224505 1 GCST90026507 no MR -> candidate analysis
Gut microbiome abundance (class Bifidobacterium animalis (at 5e-8 rs17403942 1 GCST90568939 no MR -> candidate analysis
Gut microbial network clusters (Salmon (at 1 year) x Any Bre 1e-7 rs17403620 1 GCST90569450 no MR -> candidate analysis
Suicide behavior 9e-7 rs3741042 1 GCST90244689 no MR -> candidate analysis
Crohn’s disease (Tractor method with European ancestry) 1e-6 rs117479720 1 GCST90825978 no MR -> candidate analysis
Suicide 3e-6 rs3741042 1 GCST90244688 no MR -> candidate analysis
…and 4 more traits (see JSON)          

4. Phenome map — where this gene is a genetic locus, vs. where MR exists

Top diseases by Open Targets association (of 479 total). Associations are loci, not causal claims. The causal-status column is a four-state triage per pair: established (curated) = a curated clinical assertion exists (ClinGen/G2P/GEL/Orphanet/ClinVar — any validity level, MR adds little); exploratory rare-variant signal = ExWAS burden evidence without curation — a candidate NEW gene-disease relationship; common-variant locus = GWAS signal, classic pQTL-MR territory; multi-layer = burden+GWAS together, an allelic-series candidate (the strongest causal setup). Burden estimand is carrier-vs-noncarrier, not per-SD MR.

Disease genetic assoc. burden (ExWAS) causal status MR status
hypothyroidism 0.316 common-variant locus MR: beta=-0.108, p=0.186 (cis)
thyroid gland disorder 0.289 common-variant locus no MR -> candidate analysis
Hashimoto thyroiditis 0.289 common-variant locus no MR -> candidate analysis
alcohol drinking 0.239 common-variant locus no MR -> candidate analysis
heart disorder 0.076 common-variant locus no MR -> candidate analysis
gallbladder disorder 0.069 common-variant locus no MR -> candidate analysis

Of the 6 rows above, 5 have no MR estimate in this resource. Across all retrieved diseases for this gene: 0 exploratory rare-variant signal(s), 0 multi-layer (allelic-series candidate) pair(s). Final triage still belongs to a statistical geneticist.

5. Downstream annotation (druggability & safety preview)

Layer Result
ChEMBL druggability not available — no ChEMBL target (undrugged)
gnomAD constraint not available
GWAS Catalog 93 unique SNPs / 173 rows
ClinVar 69 records; 0 pathogenic in sample of 30
PharmGKB/ClinPGx no annotations

Caveats declared by the tools

Sources

Provenance