Have questions? Visit https://www.reddit.com/r/SNPedia

rs1805094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1805094(C;C)
Make rs1805094(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position65610269
GeneLEPR
is asnp
is mentioned by
dbSNPrs1805094
ebirs1805094
HLIrs1805094
Exacrs1805094
Varsomers1805094
Maprs1805094
PheGenIrs1805094
hapmaprs1805094
1000 genomesrs1805094
hgdprs1805094
ensemblrs1805094
gopubmedrs1805094
geneviewrs1805094
scholarrs1805094
googlers1805094
pharmgkbrs1805094
gwascentralrs1805094
openSNPrs1805094
23andMers1805094
23andMe allrs1805094
SNP Nexus

SNPshotrs1805094
SNPdbers1805094
MSV3drs1805094
GWAS Ctlgrs1805094
Merged fromRs8179183
GMAF0.1446
Max Magnitude0
? (C;C) (C;G) (G;G) 28
ClinVar
Risk rs1805094(C;C)
Alt rs1805094(C;C)
Reference rs1805094(G;G)
Significance Non-pathogenic
Disease LEPTIN RECEPTOR POLYMORPHISM
Variation info
Gene LEPR LEPROT
CLNDBN LEPTIN RECEPTOR POLYMORPHISM
Reversed 0
HGVS NC_000001.10:g.66075952G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009050.2,