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rs794728416

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728416(C;T)
Make rs794728416(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150977883
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728416
ebirs794728416
HLIrs794728416
Exacrs794728416
Varsomers794728416
Maprs794728416
PheGenIrs794728416
hapmaprs794728416
1000 genomesrs794728416
hgdprs794728416
ensemblrs794728416
gopubmedrs794728416
geneviewrs794728416
scholarrs794728416
googlers794728416
pharmgkbrs794728416
gwascentralrs794728416
openSNPrs794728416
23andMers794728416
23andMe allrs794728416
SNP Nexus

SNPshotrs794728416
SNPdbers794728416
MSV3drs794728416
GWAS Ctlgrs794728416
Max Magnitude0
ClinVar
Risk rs794728416(T;T)
Alt rs794728416(T;T)
Reference rs794728416(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150674971G>A
CLNSRC
CLNACC RCV000181951.2,