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rs1057517866

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517866(A;A)
Make rs1057517866(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150951729
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057517866
dbSNP (old)rs1057517866
ClinGenrs1057517866
ebirs1057517866
HLIrs1057517866
Exacrs1057517866
Gnomadrs1057517866
Varsomers1057517866
LitVarrs1057517866
Maprs1057517866
PheGenIrs1057517866
Biobankrs1057517866
1000 genomesrs1057517866
hgdprs1057517866
ensemblrs1057517866
gopubmedrs1057517866
geneviewrs1057517866
scholarrs1057517866
googlers1057517866
pharmgkbrs1057517866
gwascentralrs1057517866
openSNPrs1057517866
23andMers1057517866
23andMe allrs1057517866
SNPshotrs1057517866
SNPdbers1057517866
MSV3drs1057517866
GWAS Ctlgrs1057517866
Max Magnitude0
ClinVar
Risk rs1057517866(A;A)
Alt rs1057517866(A;A)
Reference Rs1057517866(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648817C>T
CLNSRC
CLNACC RCV000412811.1,