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rs1064793884

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(GTTA;GTTA) 0 common in clinvar
Chromosome12
Position49043627
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1064793884
dbSNP (old)rs1064793884
ClinGenrs1064793884
ebirs1064793884
HLIrs1064793884
Exacrs1064793884
Gnomadrs1064793884
Varsomers1064793884
Maprs1064793884
PheGenIrs1064793884
Biobankrs1064793884
1000 genomesrs1064793884
hgdprs1064793884
ensemblrs1064793884
gopubmedrs1064793884
geneviewrs1064793884
scholarrs1064793884
googlers1064793884
pharmgkbrs1064793884
gwascentralrs1064793884
openSNPrs1064793884
23andMers1064793884
23andMe allrs1064793884
SNPshotrs1064793884
SNPdbers1064793884
MSV3drs1064793884
GWAS Ctlgrs1064793884
Max Magnitude0
ClinVar
Risk rs1064793884(-;-)
Alt rs1064793884(-;-)
Reference Rs1064793884(GTTA;GTTA)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49437410_49437413delTAAC
CLNSRC
CLNACC RCV000484039.1,