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rs1064796125

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position49052679
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1064796125
dbSNP (old)rs1064796125
ClinGenrs1064796125
ebirs1064796125
HLIrs1064796125
Exacrs1064796125
Gnomadrs1064796125
Varsomers1064796125
LitVarrs1064796125
Maprs1064796125
PheGenIrs1064796125
Biobankrs1064796125
1000 genomesrs1064796125
hgdprs1064796125
ensemblrs1064796125
gopubmedrs1064796125
geneviewrs1064796125
scholarrs1064796125
googlers1064796125
pharmgkbrs1064796125
gwascentralrs1064796125
openSNPrs1064796125
23andMers1064796125
23andMe allrs1064796125
SNPshotrs1064796125
SNPdbers1064796125
MSV3drs1064796125
GWAS Ctlgrs1064796125
Max Magnitude0
ClinVar
Risk rs1064796125(-;-)
Alt rs1064796125(-;-)
Reference Rs1064796125(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49446462delG
CLNSRC
CLNACC RCV000482724.1,