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rs794728442

From SNPedia

Orientationminus
Make rs794728442(-;-)
Make rs794728442(-;AGA)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150951478
GeneKCNH2
is asnp
is mentioned by
dbSNPrs794728442
ebirs794728442
HLIrs794728442
Exacrs794728442
Varsomers794728442
Maprs794728442
PheGenIrs794728442
hapmaprs794728442
1000 genomesrs794728442
hgdprs794728442
ensemblrs794728442
gopubmedrs794728442
geneviewrs794728442
scholarrs794728442
googlers794728442
pharmgkbrs794728442
gwascentralrs794728442
openSNPrs794728442
23andMers794728442
23andMe allrs794728442
SNP Nexus

SNPshotrs794728442
SNPdbers794728442
MSV3drs794728442
GWAS Ctlgrs794728442
Max Magnitude
ClinVar
Risk rs794728442(;)
Alt rs794728442(;)
Reference rs794728442(AGA;AGA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648566_150648568delTCT
CLNSRC
CLNACC RCV000181980.2,