Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728411

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728411(C;T)
Make rs794728411(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974804
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728411
ebirs794728411
HLIrs794728411
Exacrs794728411
Varsomers794728411
Maprs794728411
PheGenIrs794728411
hapmaprs794728411
1000 genomesrs794728411
hgdprs794728411
ensemblrs794728411
gopubmedrs794728411
geneviewrs794728411
scholarrs794728411
googlers794728411
pharmgkbrs794728411
gwascentralrs794728411
openSNPrs794728411
23andMers794728411
23andMe allrs794728411
SNP Nexus

SNPshotrs794728411
SNPdbers794728411
MSV3drs794728411
GWAS Ctlgrs794728411
Max Magnitude0
ClinVar
Risk rs794728411(T;T)
Alt rs794728411(T;T)
Reference rs794728411(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150671892G>A
CLNSRC
CLNACC RCV000181936.1,