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rs1064796300

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TGCTGAAAC;TGCTGAAAC) 0 common in clinvar
Chromosome12
Position49030904
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1064796300
dbSNP (old)rs1064796300
ClinGenrs1064796300
ebirs1064796300
HLIrs1064796300
Exacrs1064796300
Gnomadrs1064796300
Varsomers1064796300
Maprs1064796300
PheGenIrs1064796300
Biobankrs1064796300
1000 genomesrs1064796300
hgdprs1064796300
ensemblrs1064796300
gopubmedrs1064796300
geneviewrs1064796300
scholarrs1064796300
googlers1064796300
pharmgkbrs1064796300
gwascentralrs1064796300
openSNPrs1064796300
23andMers1064796300
23andMe allrs1064796300
SNPshotrs1064796300
SNPdbers1064796300
MSV3drs1064796300
GWAS Ctlgrs1064796300
Max Magnitude0
ClinVar
Risk rs1064796300(-;-)
Alt rs1064796300(-;-)
Reference Rs1064796300(TGCTGAAAC;TGCTGAAAC)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49424687_49424695delGTTTCAGCA
CLNSRC
CLNACC RCV000479574.1,