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rs1057517743

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517743(-;-)
Make rs1057517743(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150947381
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057517743
dbSNP (old)rs1057517743
ClinGenrs1057517743
ebirs1057517743
HLIrs1057517743
Exacrs1057517743
Gnomadrs1057517743
Varsomers1057517743
LitVarrs1057517743
Maprs1057517743
PheGenIrs1057517743
Biobankrs1057517743
1000 genomesrs1057517743
hgdprs1057517743
ensemblrs1057517743
gopubmedrs1057517743
geneviewrs1057517743
scholarrs1057517743
googlers1057517743
pharmgkbrs1057517743
gwascentralrs1057517743
openSNPrs1057517743
23andMers1057517743
23andMe allrs1057517743
SNPshotrs1057517743
SNPdbers1057517743
MSV3drs1057517743
GWAS Ctlgrs1057517743
Max Magnitude0
ClinVar
Risk rs1057517743(-;-)
Alt rs1057517743(-;-)
Reference Rs1057517743(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644469delC
CLNSRC
CLNACC RCV000414670.1,