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

rs794728480

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728480(A;A)
Make rs794728480(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951591
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728480
ebirs794728480
HLIrs794728480
Exacrs794728480
Varsomers794728480
Maprs794728480
PheGenIrs794728480
hapmaprs794728480
1000 genomesrs794728480
hgdprs794728480
ensemblrs794728480
gopubmedrs794728480
geneviewrs794728480
scholarrs794728480
googlers794728480
pharmgkbrs794728480
gwascentralrs794728480
openSNPrs794728480
23andMers794728480
23andMe allrs794728480
SNP Nexus

SNPshotrs794728480
SNPdbers794728480
MSV3drs794728480
GWAS Ctlgrs794728480
Max Magnitude0
ClinVar
Risk rs794728480(A;A)
Alt rs794728480(A;A)
Reference rs794728480(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648679C>T
CLNSRC
CLNACC RCV000182024.2,