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rs563611707

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs563611707(A;A)
Make rs563611707(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position150974744
GeneKCNH2
is asnp
is mentioned by
dbSNPrs563611707
ebirs563611707
HLIrs563611707
Exacrs563611707
Varsomers563611707
Maprs563611707
PheGenIrs563611707
hapmaprs563611707
1000 genomesrs563611707
hgdprs563611707
ensemblrs563611707
gopubmedrs563611707
geneviewrs563611707
scholarrs563611707
googlers563611707
pharmgkbrs563611707
gwascentralrs563611707
openSNPrs563611707
23andMers563611707
23andMe allrs563611707
SNP Nexus

SNPshotrs563611707
SNPdbers563611707
MSV3drs563611707
GWAS Ctlgrs563611707
Max Magnitude0
ClinVar
Risk rs563611707(A;A)
Alt rs563611707(A;A)
Reference rs563611707(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.150671832G>A
CLNSRC
CLNACC RCV000181942.1,