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rs377095107

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377095107(A;A)
Make rs377095107(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150947341
GeneKCNH2
is asnp
is mentioned by
dbSNPrs377095107
ebirs377095107
HLIrs377095107
Exacrs377095107
Varsomers377095107
Maprs377095107
PheGenIrs377095107
hapmaprs377095107
1000 genomesrs377095107
hgdprs377095107
ensemblrs377095107
gopubmedrs377095107
geneviewrs377095107
scholarrs377095107
googlers377095107
pharmgkbrs377095107
gwascentralrs377095107
openSNPrs377095107
23andMers377095107
23andMe allrs377095107
SNP Nexus

SNPshotrs377095107
SNPdbers377095107
MSV3drs377095107
GWAS Ctlgrs377095107
Max Magnitude0
ClinVar
Risk rs377095107(A;A)
Alt rs377095107(A;A)
Reference rs377095107(G;G)
Significance Probable-Pathogenic
Disease Long QT syndrome not specified
Variation info
Gene KCNH2
CLNDBN Long QT syndrome not specified
Reversed 0
HGVS NC_000007.13:g.150644429G>A
CLNSRC
CLNACC RCV000148531.1, RCV000181913.2,