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rs1085307620

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TGGCA;TGGCA) 0 common in clinvar
Chromosome7
Position150958306
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1085307620
dbSNP (old)rs1085307620
ClinGenrs1085307620
ebirs1085307620
HLIrs1085307620
Exacrs1085307620
Gnomadrs1085307620
Varsomers1085307620
Maprs1085307620
PheGenIrs1085307620
Biobankrs1085307620
1000 genomesrs1085307620
hgdprs1085307620
ensemblrs1085307620
gopubmedrs1085307620
geneviewrs1085307620
scholarrs1085307620
googlers1085307620
pharmgkbrs1085307620
gwascentralrs1085307620
openSNPrs1085307620
23andMers1085307620
23andMe allrs1085307620
SNPshotrs1085307620
SNPdbers1085307620
MSV3drs1085307620
GWAS Ctlgrs1085307620
Max Magnitude0
ClinVar
Risk rs1085307620(C;C)
Alt rs1085307620(C;C)
Reference Rs1085307620(TGGCA;TGGCA)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150655394_150655398delTGCCAinsG
CLNSRC
CLNACC RCV000489511.1,