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rs794728485

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728485(A;T)
Make rs794728485(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951556
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728485
ebirs794728485
HLIrs794728485
Exacrs794728485
Varsomers794728485
Maprs794728485
PheGenIrs794728485
hapmaprs794728485
1000 genomesrs794728485
hgdprs794728485
ensemblrs794728485
gopubmedrs794728485
geneviewrs794728485
scholarrs794728485
googlers794728485
pharmgkbrs794728485
gwascentralrs794728485
openSNPrs794728485
23andMers794728485
23andMe allrs794728485
SNP Nexus

SNPshotrs794728485
SNPdbers794728485
MSV3drs794728485
GWAS Ctlgrs794728485
Max Magnitude0
ClinVar
Risk rs794728485(T;T)
Alt rs794728485(T;T)
Reference rs794728485(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648644T>A
CLNSRC
CLNACC RCV000182031.1,