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rs1085307943

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position150951096
GeneKCNH2
is asnp
is mentioned by
dbSNPrs1085307943
dbSNP (old)rs1085307943
ClinGenrs1085307943
ebirs1085307943
HLIrs1085307943
Exacrs1085307943
Gnomadrs1085307943
Varsomers1085307943
Maprs1085307943
PheGenIrs1085307943
Biobankrs1085307943
1000 genomesrs1085307943
hgdprs1085307943
ensemblrs1085307943
gopubmedrs1085307943
geneviewrs1085307943
scholarrs1085307943
googlers1085307943
pharmgkbrs1085307943
gwascentralrs1085307943
openSNPrs1085307943
23andMers1085307943
23andMe allrs1085307943
SNPshotrs1085307943
SNPdbers1085307943
MSV3drs1085307943
GWAS Ctlgrs1085307943
Max Magnitude0
ClinVar
Risk rs1085307943(T;T)
Alt rs1085307943(T;T)
Reference Rs1085307943(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.150648184C>A
CLNSRC
CLNACC RCV000490005.1,