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rs1057520558

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520558(C;G)
Make rs1057520558(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150947453
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057520558
dbSNP (old)rs1057520558
ClinGenrs1057520558
ebirs1057520558
HLIrs1057520558
Exacrs1057520558
Gnomadrs1057520558
Varsomers1057520558
Maprs1057520558
PheGenIrs1057520558
Biobankrs1057520558
1000 genomesrs1057520558
hgdprs1057520558
ensemblrs1057520558
gopubmedrs1057520558
geneviewrs1057520558
scholarrs1057520558
googlers1057520558
pharmgkbrs1057520558
gwascentralrs1057520558
openSNPrs1057520558
23andMers1057520558
23andMe allrs1057520558
SNPshotrs1057520558
SNPdbers1057520558
MSV3drs1057520558
GWAS Ctlgrs1057520558
Max Magnitude0
ClinVar
Risk rs1057520558(G;G)
Alt rs1057520558(G;G)
Reference Rs1057520558(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644541G>C
CLNSRC
CLNACC RCV000423718.1,