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rs193922697

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922697(A;A)
Make rs193922697(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position151576438
GenePRKAG2
is asnp
is mentioned by
dbSNPrs193922697
ebirs193922697
HLIrs193922697
Exacrs193922697
Varsomers193922697
Maprs193922697
PheGenIrs193922697
hapmaprs193922697
1000 genomesrs193922697
hgdprs193922697
ensemblrs193922697
gopubmedrs193922697
geneviewrs193922697
scholarrs193922697
googlers193922697
pharmgkbrs193922697
gwascentralrs193922697
openSNPrs193922697
23andMers193922697
23andMe allrs193922697
SNP Nexus

SNPshotrs193922697
SNPdbers193922697
MSV3drs193922697
GWAS Ctlgrs193922697
Max Magnitude0
ClinVar
Risk rs193922697(A,T;A,T)
Alt rs193922697(A,T;A,T)
Reference rs193922697(C;C)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene PRKAG2
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000007.13:g.151273524G>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030377.1,