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rs1064793748

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position137716895
GeneEHMT1
is asnp
is mentioned by
dbSNPrs1064793748
dbSNP (classic)rs1064793748
ClinGenrs1064793748
ebirs1064793748
HLIrs1064793748
Exacrs1064793748
Gnomadrs1064793748
Varsomers1064793748
LitVarrs1064793748
Maprs1064793748
PheGenIrs1064793748
Biobankrs1064793748
1000 genomesrs1064793748
hgdprs1064793748
ensemblrs1064793748
geneviewrs1064793748
scholarrs1064793748
googlers1064793748
pharmgkbrs1064793748
gwascentralrs1064793748
openSNPrs1064793748
23andMers1064793748
23andMe allrs1064793748
SNPshotrs1064793748
SNPdbers1064793748
MSV3drs1064793748
GWAS Ctlgrs1064793748
Max Magnitude0
ClinVar
Risk rs1064793748(-;-)
Alt rs1064793748(-;-)
Reference Rs1064793748(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene EHMT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140611347delG
CLNSRC
CLNACC RCV000487296.1,