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rs794728370

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728370(G;G)
Make rs794728370(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952486
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728370
ebirs794728370
HLIrs794728370
Exacrs794728370
Varsomers794728370
Maprs794728370
PheGenIrs794728370
hapmaprs794728370
1000 genomesrs794728370
hgdprs794728370
ensemblrs794728370
gopubmedrs794728370
geneviewrs794728370
scholarrs794728370
googlers794728370
pharmgkbrs794728370
gwascentralrs794728370
openSNPrs794728370
23andMers794728370
23andMe allrs794728370
SNP Nexus

SNPshotrs794728370
SNPdbers794728370
MSV3drs794728370
GWAS Ctlgrs794728370
Max Magnitude0
ClinVar
Risk rs794728370(G;G)
Alt rs794728370(G;G)
Reference rs794728370(T;T)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene KCNH2
CLNDBN not provided not specified
Reversed 1
HGVS NC_000007.13:g.150649574A>C
CLNSRC
CLNACC RCV000181793.2, RCV000223922.1,