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

rs387907025

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387907025(C;T)
Make rs387907025(T;T)
ReferenceGRCh37.p10 37.5/138
Chromosome7
Position141341162
GeneAGK
is asnp
is mentioned by
dbSNPrs387907025
ebirs387907025
HLIrs387907025
Exacrs387907025
Varsomers387907025
Maprs387907025
PheGenIrs387907025
hapmaprs387907025
1000 genomesrs387907025
hgdprs387907025
ensemblrs387907025
gopubmedrs387907025
geneviewrs387907025
scholarrs387907025
googlers387907025
pharmgkbrs387907025
gwascentralrs387907025
openSNPrs387907025
23andMers387907025
23andMe allrs387907025
SNP Nexus

SNPshotrs387907025
SNPdbers387907025
MSV3drs387907025
GWAS Ctlgrs387907025
Max Magnitude0
ClinVar
Risk rs387907025(T;T)
Alt rs387907025(T;T)
Reference rs387907025(C;C)
Significance Pathogenic
Disease Cataract and cardiomyopathy
Variation info
Gene AGK
CLNDBN Cataract and cardiomyopathy
Reversed 0
HGVS NC_000007.13:g.141341162C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023814.3,