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rs794728360

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728360(A;A)
Make rs794728360(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150958226
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728360
ebirs794728360
HLIrs794728360
Exacrs794728360
Varsomers794728360
Maprs794728360
PheGenIrs794728360
hapmaprs794728360
1000 genomesrs794728360
hgdprs794728360
ensemblrs794728360
gopubmedrs794728360
geneviewrs794728360
scholarrs794728360
googlers794728360
pharmgkbrs794728360
gwascentralrs794728360
openSNPrs794728360
23andMers794728360
23andMe allrs794728360
SNP Nexus

SNPshotrs794728360
SNPdbers794728360
MSV3drs794728360
GWAS Ctlgrs794728360
Max Magnitude0
ClinVar
Risk rs794728360(A;A)
Alt rs794728360(A;A)
Reference rs794728360(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150655314G>T
CLNSRC
CLNACC RCV000181766.1,