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rs1057520477

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520477(C;G)
Make rs1057520477(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150951707
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057520477
dbSNP (old)rs1057520477
ClinGenrs1057520477
ebirs1057520477
HLIrs1057520477
Exacrs1057520477
Gnomadrs1057520477
Varsomers1057520477
Maprs1057520477
PheGenIrs1057520477
Biobankrs1057520477
1000 genomesrs1057520477
hgdprs1057520477
ensemblrs1057520477
gopubmedrs1057520477
geneviewrs1057520477
scholarrs1057520477
googlers1057520477
pharmgkbrs1057520477
gwascentralrs1057520477
openSNPrs1057520477
23andMers1057520477
23andMe allrs1057520477
SNPshotrs1057520477
SNPdbers1057520477
MSV3drs1057520477
GWAS Ctlgrs1057520477
Max Magnitude0
ClinVar
Risk rs1057520477(G;G)
Alt rs1057520477(G;G)
Reference Rs1057520477(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648795G>C
CLNSRC
CLNACC RCV000434772.1,