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rs1057518169

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518169(C;C)
Make rs1057518169(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150947326
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057518169
dbSNP (old)rs1057518169
ClinGenrs1057518169
ebirs1057518169
HLIrs1057518169
Exacrs1057518169
Gnomadrs1057518169
Varsomers1057518169
LitVarrs1057518169
Maprs1057518169
PheGenIrs1057518169
Biobankrs1057518169
1000 genomesrs1057518169
hgdprs1057518169
ensemblrs1057518169
gopubmedrs1057518169
geneviewrs1057518169
scholarrs1057518169
googlers1057518169
pharmgkbrs1057518169
gwascentralrs1057518169
openSNPrs1057518169
23andMers1057518169
23andMe allrs1057518169
SNPshotrs1057518169
SNPdbers1057518169
MSV3drs1057518169
GWAS Ctlgrs1057518169
Max Magnitude0
ClinVar
Risk rs1057518169(C;C)
Alt rs1057518169(C;C)
Reference Rs1057518169(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644414A>G
CLNSRC
CLNACC RCV000413963.1,