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rs1057518151

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518151(G;T)
Make rs1057518151(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position150947327
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1057518151
dbSNP (old)rs1057518151
ClinGenrs1057518151
ebirs1057518151
HLIrs1057518151
Exacrs1057518151
Gnomadrs1057518151
Varsomers1057518151
Maprs1057518151
PheGenIrs1057518151
Biobankrs1057518151
1000 genomesrs1057518151
hgdprs1057518151
ensemblrs1057518151
gopubmedrs1057518151
geneviewrs1057518151
scholarrs1057518151
googlers1057518151
pharmgkbrs1057518151
gwascentralrs1057518151
openSNPrs1057518151
23andMers1057518151
23andMe allrs1057518151
SNPshotrs1057518151
SNPdbers1057518151
MSV3drs1057518151
GWAS Ctlgrs1057518151
Max Magnitude0
ClinVar
Risk rs1057518151(T;T)
Alt rs1057518151(T;T)
Reference Rs1057518151(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150644415C>A
CLNSRC
CLNACC RCV000414266.1,