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rs1057523338

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057523338(A;G)
Make rs1057523338(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150951093
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057523338
dbSNP (old)rs1057523338
ClinGenrs1057523338
ebirs1057523338
HLIrs1057523338
Exacrs1057523338
Gnomadrs1057523338
Varsomers1057523338
Maprs1057523338
PheGenIrs1057523338
Biobankrs1057523338
1000 genomesrs1057523338
hgdprs1057523338
ensemblrs1057523338
gopubmedrs1057523338
geneviewrs1057523338
scholarrs1057523338
googlers1057523338
pharmgkbrs1057523338
gwascentralrs1057523338
openSNPrs1057523338
23andMers1057523338
23andMe allrs1057523338
SNPshotrs1057523338
SNPdbers1057523338
MSV3drs1057523338
GWAS Ctlgrs1057523338
Max Magnitude0
ClinVar
Risk rs1057523338(G;G)
Alt rs1057523338(G;G)
Reference Rs1057523338(A;A)
Significance Probable-Pathogenic
Disease not provided Long QT syndrome
Variation info
Gene KCNH2
CLNDBN not provided Long QT syndrome
Reversed 1
HGVS NC_000007.13:g.150648181T>C
CLNSRC
CLNACC RCV000426599.1, RCV000466780.1,