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rs1057522921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057522921(G;T)
Make rs1057522921(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150948439
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057522921
dbSNP (old)rs1057522921
ClinGenrs1057522921
ebirs1057522921
HLIrs1057522921
Exacrs1057522921
Gnomadrs1057522921
Varsomers1057522921
Maprs1057522921
PheGenIrs1057522921
Biobankrs1057522921
1000 genomesrs1057522921
hgdprs1057522921
ensemblrs1057522921
gopubmedrs1057522921
geneviewrs1057522921
scholarrs1057522921
googlers1057522921
pharmgkbrs1057522921
gwascentralrs1057522921
openSNPrs1057522921
23andMers1057522921
23andMe allrs1057522921
SNPshotrs1057522921
SNPdbers1057522921
MSV3drs1057522921
GWAS Ctlgrs1057522921
Max Magnitude0
ClinVar
Risk rs1057522921(T;T)
Alt rs1057522921(T;T)
Reference Rs1057522921(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150645527C>A
CLNSRC
CLNACC RCV000418102.1,