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rs1064793368

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome7
Position150949033
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1064793368
dbSNP (old)rs1064793368
ClinGenrs1064793368
ebirs1064793368
HLIrs1064793368
Exacrs1064793368
Gnomadrs1064793368
Varsomers1064793368
Maprs1064793368
PheGenIrs1064793368
Biobankrs1064793368
1000 genomesrs1064793368
hgdprs1064793368
ensemblrs1064793368
gopubmedrs1064793368
geneviewrs1064793368
scholarrs1064793368
googlers1064793368
pharmgkbrs1064793368
gwascentralrs1064793368
openSNPrs1064793368
23andMers1064793368
23andMe allrs1064793368
SNPshotrs1064793368
SNPdbers1064793368
MSV3drs1064793368
GWAS Ctlgrs1064793368
Max Magnitude0
ClinVar
Risk rs1064793368(-;-)
Alt rs1064793368(-;-)
Reference Rs1064793368(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150646121delA
CLNSRC
CLNACC RCV000480935.1,