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rs1057518089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518089(-;T)
Make rs1057518089(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150947006
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057518089
dbSNP (old)rs1057518089
ClinGenrs1057518089
ebirs1057518089
HLIrs1057518089
Exacrs1057518089
Gnomadrs1057518089
Varsomers1057518089
Maprs1057518089
PheGenIrs1057518089
Biobankrs1057518089
1000 genomesrs1057518089
hgdprs1057518089
ensemblrs1057518089
gopubmedrs1057518089
geneviewrs1057518089
scholarrs1057518089
googlers1057518089
pharmgkbrs1057518089
gwascentralrs1057518089
openSNPrs1057518089
23andMers1057518089
23andMe allrs1057518089
SNPshotrs1057518089
SNPdbers1057518089
MSV3drs1057518089
GWAS Ctlgrs1057518089
Max Magnitude0
ClinVar
Risk rs1057518089(T;T)
Alt rs1057518089(T;T)
Reference Rs1057518089(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644095dupA
CLNSRC
CLNACC RCV000414739.1,