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rs41307295

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41307295(A;A)
Make rs41307295(A;G)
ReferenceGRCh38 38.1/142
Chromosome7
Position150951506
GeneKCNH2
is asnp
is mentioned by
dbSNPrs41307295
ebirs41307295
HLIrs41307295
Exacrs41307295
Varsomers41307295
Maprs41307295
PheGenIrs41307295
hapmaprs41307295
1000 genomesrs41307295
hgdprs41307295
ensemblrs41307295
gopubmedrs41307295
geneviewrs41307295
scholarrs41307295
googlers41307295
pharmgkbrs41307295
gwascentralrs41307295
openSNPrs41307295
23andMers41307295
23andMe allrs41307295
SNP Nexus

SNPshotrs41307295
SNPdbers41307295
MSV3drs41307295
GWAS Ctlgrs41307295
Max Magnitude0
ClinVar
Risk rs41307295(A,T;A,T)
Alt rs41307295(A,T;A,T)
Reference rs41307295(G;G)
Significance Pathogenic
Disease Congenital long QT syndrome
Variation info
Gene KCNH2
CLNDBN Congenital long QT syndrome
Reversed 0
HGVS NC_000007.13:g.150648594G>T
CLNSRC ClinVar
CLNACC RCV000058036.2,