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rs121908990

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908990(C;G)
Make rs121908990(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position151560611
GenePRKAG2
is asnp
is mentioned by
dbSNPrs121908990
ebirs121908990
HLIrs121908990
Exacrs121908990
Varsomers121908990
Maprs121908990
PheGenIrs121908990
hapmaprs121908990
1000 genomesrs121908990
hgdprs121908990
ensemblrs121908990
gopubmedrs121908990
geneviewrs121908990
scholarrs121908990
googlers121908990
pharmgkbrs121908990
gwascentralrs121908990
openSNPrs121908990
23andMers121908990
23andMe allrs121908990
SNP Nexus

SNPshotrs121908990
SNPdbers121908990
MSV3drs121908990
GWAS Ctlgrs121908990
Max Magnitude0
OMIM602743
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908990(G,T;G,T)
Alt rs121908990(G,T;G,T)
Reference rs121908990(C;C)
Significance Pathogenic
Disease Wolff-Parkinson-White syndrome
Variation info
Gene PRKAG2
CLNDBN Wolff-Parkinson-White syndrome, childhood-onset
Reversed 1
HGVS NC_000007.13:g.151257697G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007254.3,