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rs1064796672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome11
Position118493168
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1064796672
dbSNP (old)rs1064796672
ClinGenrs1064796672
ebirs1064796672
HLIrs1064796672
Exacrs1064796672
Gnomadrs1064796672
Varsomers1064796672
Maprs1064796672
PheGenIrs1064796672
Biobankrs1064796672
1000 genomesrs1064796672
hgdprs1064796672
ensemblrs1064796672
gopubmedrs1064796672
geneviewrs1064796672
scholarrs1064796672
googlers1064796672
pharmgkbrs1064796672
gwascentralrs1064796672
openSNPrs1064796672
23andMers1064796672
23andMe allrs1064796672
SNPshotrs1064796672
SNPdbers1064796672
MSV3drs1064796672
GWAS Ctlgrs1064796672
Max Magnitude0
ClinVar
Risk rs1064796672(-;-)
Alt rs1064796672(-;-)
Reference Rs1064796672(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118363883delC
CLNSRC
CLNACC RCV000481855.1,