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rs764831888

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs764831888(C;C)
Make rs764831888(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150959657
GeneKCNH2
is asnp
is mentioned by
dbSNPrs764831888
ebirs764831888
HLIrs764831888
Exacrs764831888
Varsomers764831888
Maprs764831888
PheGenIrs764831888
hapmaprs764831888
1000 genomesrs764831888
hgdprs764831888
ensemblrs764831888
gopubmedrs764831888
geneviewrs764831888
scholarrs764831888
googlers764831888
pharmgkbrs764831888
gwascentralrs764831888
openSNPrs764831888
23andMers764831888
23andMe allrs764831888
SNP Nexus

SNPshotrs764831888
SNPdbers764831888
MSV3drs764831888
GWAS Ctlgrs764831888
Max Magnitude0
ClinVar
Risk rs764831888(A,C;A,C)
Alt rs764831888(A,C;A,C)
Reference rs764831888(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.150656745G>C
CLNSRC
CLNACC RCV000181754.2,