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

rs746709222

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs746709222(C;T)
Make rs746709222(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position141614164
GeneAGK
is asnp
is mentioned by
dbSNPrs746709222
ebirs746709222
HLIrs746709222
Exacrs746709222
Varsomers746709222
Maprs746709222
PheGenIrs746709222
hapmaprs746709222
1000 genomesrs746709222
hgdprs746709222
ensemblrs746709222
gopubmedrs746709222
geneviewrs746709222
scholarrs746709222
googlers746709222
pharmgkbrs746709222
gwascentralrs746709222
openSNPrs746709222
23andMers746709222
23andMe allrs746709222
SNP Nexus

SNPshotrs746709222
SNPdbers746709222
MSV3drs746709222
GWAS Ctlgrs746709222
Max Magnitude0
ClinVar
Risk rs746709222(T;T)
Alt rs746709222(T;T)
Reference rs746709222(C;C)
Significance Pathogenic
Disease Cataract and cardiomyopathy
Variation info
Gene AGK
CLNDBN Cataract and cardiomyopathy
Reversed 0
HGVS NC_000007.13:g.141313964C>T
CLNSRC Baylor College of Medicine
CLNACC RCV000191059.1,