Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064796776

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome11
Position118494755
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1064796776
dbSNP (old)rs1064796776
ClinGenrs1064796776
ebirs1064796776
HLIrs1064796776
Exacrs1064796776
Gnomadrs1064796776
Varsomers1064796776
Maprs1064796776
PheGenIrs1064796776
Biobankrs1064796776
1000 genomesrs1064796776
hgdprs1064796776
ensemblrs1064796776
gopubmedrs1064796776
geneviewrs1064796776
scholarrs1064796776
googlers1064796776
pharmgkbrs1064796776
gwascentralrs1064796776
openSNPrs1064796776
23andMers1064796776
23andMe allrs1064796776
SNPshotrs1064796776
SNPdbers1064796776
MSV3drs1064796776
GWAS Ctlgrs1064796776
Max Magnitude0
ClinVar
Risk rs1064796776(G;G)
Alt rs1064796776(G;G)
Reference Rs1064796776(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118365470A>G
CLNSRC
CLNACC RCV000486341.1,