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rs1064796996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position137813477
GeneEHMT1
is asnp
is mentioned by
dbSNPrs1064796996
dbSNP (old)rs1064796996
ClinGenrs1064796996
ebirs1064796996
HLIrs1064796996
Exacrs1064796996
Gnomadrs1064796996
Varsomers1064796996
LitVarrs1064796996
Maprs1064796996
PheGenIrs1064796996
Biobankrs1064796996
1000 genomesrs1064796996
hgdprs1064796996
ensemblrs1064796996
gopubmedrs1064796996
geneviewrs1064796996
scholarrs1064796996
googlers1064796996
pharmgkbrs1064796996
gwascentralrs1064796996
openSNPrs1064796996
23andMers1064796996
23andMe allrs1064796996
SNPshotrs1064796996
SNPdbers1064796996
MSV3drs1064796996
GWAS Ctlgrs1064796996
Max Magnitude0
ClinVar
Risk rs1064796996(T;T)
Alt rs1064796996(T;T)
Reference Rs1064796996(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene EHMT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.140707929C>T
CLNSRC
CLNACC RCV000479136.1,