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rs137853228

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853228(A;A)
Make rs137853228(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position50256729
GeneGNAI2
is asnp
is mentioned by
dbSNPrs137853228
ebirs137853228
HLIrs137853228
Exacrs137853228
Varsomers137853228
Maprs137853228
PheGenIrs137853228
hapmaprs137853228
1000 genomesrs137853228
hgdprs137853228
ensemblrs137853228
gopubmedrs137853228
geneviewrs137853228
scholarrs137853228
googlers137853228
pharmgkbrs137853228
gwascentralrs137853228
openSNPrs137853228
23andMers137853228
23andMe allrs137853228
SNP Nexus

SNPshotrs137853228
SNPdbers137853228
MSV3drs137853228
GWAS Ctlgrs137853228
Max Magnitude0
OMIM139360
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853228(A;A)
Alt rs137853228(A;A)
Reference rs137853228(T;T)
Significance Pathogenic
Disease Ventricular tachycardia
Variation info
Gene GNAI2
CLNDBN Ventricular tachycardia, somatic
Reversed 0
HGVS NC_000003.11:g.50294161T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017257.4,