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rs149955375

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149955375(A;A)
Make rs149955375(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150947623
GeneKCNH2
is asnp
is mentioned by
dbSNPrs149955375
ebirs149955375
HLIrs149955375
Exacrs149955375
Varsomers149955375
Maprs149955375
PheGenIrs149955375
hapmaprs149955375
1000 genomesrs149955375
hgdprs149955375
ensemblrs149955375
gopubmedrs149955375
geneviewrs149955375
scholarrs149955375
googlers149955375
pharmgkbrs149955375
gwascentralrs149955375
openSNPrs149955375
23andMers149955375
23andMe allrs149955375
SNP Nexus

SNPshotrs149955375
SNPdbers149955375
MSV3drs149955375
GWAS Ctlgrs149955375
Max Magnitude0
ClinVar
Risk rs149955375(A;A)
Alt rs149955375(A;A)
Reference rs149955375(G;G)
Significance Other
Disease Congenital long QT syndrome Long QT syndrome not provided not specified
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome Long QT syndrome not provided not specified
Reversed 0
HGVS NC_000007.13:g.150644711G>A
CLNSRC ClinVar University of Washington
CLNACC RCV000058182.2, RCV000148532.3, RCV000174225.1, RCV000181901.3,