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rs1085307734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Chromosome9
Position137813422
GeneEHMT1
is asnp
is mentioned by
dbSNPrs1085307734
dbSNP (old)rs1085307734
ClinGenrs1085307734
ebirs1085307734
HLIrs1085307734
Exacrs1085307734
Gnomadrs1085307734
Varsomers1085307734
LitVarrs1085307734
Maprs1085307734
PheGenIrs1085307734
Biobankrs1085307734
1000 genomesrs1085307734
hgdprs1085307734
ensemblrs1085307734
gopubmedrs1085307734
geneviewrs1085307734
scholarrs1085307734
googlers1085307734
pharmgkbrs1085307734
gwascentralrs1085307734
openSNPrs1085307734
23andMers1085307734
23andMe allrs1085307734
SNPshotrs1085307734
SNPdbers1085307734
MSV3drs1085307734
GWAS Ctlgrs1085307734
Max Magnitude0
ClinVar
Risk rs1085307734(-;-)
Alt rs1085307734(-;-)
Reference Rs1085307734(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene EHMT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140707874_140707875delCT
CLNSRC
CLNACC RCV000489264.1,