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rs201268831

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201268831(A;A)
Make rs201268831(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150952652
GeneKCNH2
is asnp
is mentioned by
dbSNPrs201268831
ebirs201268831
HLIrs201268831
Exacrs201268831
Varsomers201268831
Maprs201268831
PheGenIrs201268831
hapmaprs201268831
1000 genomesrs201268831
hgdprs201268831
ensemblrs201268831
gopubmedrs201268831
geneviewrs201268831
scholarrs201268831
googlers201268831
pharmgkbrs201268831
gwascentralrs201268831
openSNPrs201268831
23andMers201268831
23andMe allrs201268831
SNP Nexus

SNPshotrs201268831
SNPdbers201268831
MSV3drs201268831
GWAS Ctlgrs201268831
Max Magnitude0
ClinVar
Risk rs201268831(A,T;A,T)
Alt rs201268831(A,T;A,T)
Reference rs201268831(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.150649740C>A; NC_000007.13:g.150649740C>T
CLNSRC
CLNACC RCV000181788.2, RCV000171665.1,