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

rs587777604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777604(C;G)
Make rs587777604(G;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position25317064
GeneABHD12
is asnp
is mentioned by
dbSNPrs587777604
ebirs587777604
HLIrs587777604
Exacrs587777604
Varsomers587777604
Maprs587777604
PheGenIrs587777604
hapmaprs587777604
1000 genomesrs587777604
hgdprs587777604
ensemblrs587777604
gopubmedrs587777604
geneviewrs587777604
scholarrs587777604
googlers587777604
pharmgkbrs587777604
gwascentralrs587777604
openSNPrs587777604
23andMers587777604
23andMe allrs587777604
SNP Nexus

SNPshotrs587777604
SNPdbers587777604
MSV3drs587777604
GWAS Ctlgrs587777604
Max Magnitude0
ClinVar
Risk rs587777604(G,T;G,T)
Alt rs587777604(G,T;G,T)
Reference rs587777604(C;C)
Significance Pathogenic
Disease Polyneuropathy
Variation info
Gene ABHD12
CLNDBN Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract
Reversed 0
HGVS NC_000020.10:g.25297700C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000132769.3,