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rs1085307748

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position137716842
GeneEHMT1
is asnp
is mentioned by
dbSNPrs1085307748
dbSNP (old)rs1085307748
ClinGenrs1085307748
ebirs1085307748
HLIrs1085307748
Exacrs1085307748
Gnomadrs1085307748
Varsomers1085307748
Maprs1085307748
PheGenIrs1085307748
Biobankrs1085307748
1000 genomesrs1085307748
hgdprs1085307748
ensemblrs1085307748
gopubmedrs1085307748
geneviewrs1085307748
scholarrs1085307748
googlers1085307748
pharmgkbrs1085307748
gwascentralrs1085307748
openSNPrs1085307748
23andMers1085307748
23andMe allrs1085307748
SNPshotrs1085307748
SNPdbers1085307748
MSV3drs1085307748
GWAS Ctlgrs1085307748
Max Magnitude0
ClinVar
Risk rs1085307748(G;G)
Alt rs1085307748(G;G)
Reference Rs1085307748(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene EHMT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140611294C>G
CLNSRC
CLNACC RCV000489688.1,