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

rs1064796995

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position49050970
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1064796995
dbSNP (old)rs1064796995
ClinGenrs1064796995
ebirs1064796995
HLIrs1064796995
Exacrs1064796995
Gnomadrs1064796995
Varsomers1064796995
Maprs1064796995
PheGenIrs1064796995
Biobankrs1064796995
1000 genomesrs1064796995
hgdprs1064796995
ensemblrs1064796995
gopubmedrs1064796995
geneviewrs1064796995
scholarrs1064796995
googlers1064796995
pharmgkbrs1064796995
gwascentralrs1064796995
openSNPrs1064796995
23andMers1064796995
23andMe allrs1064796995
SNPshotrs1064796995
SNPdbers1064796995
MSV3drs1064796995
GWAS Ctlgrs1064796995
Max Magnitude0
ClinVar
Risk rs1064796995(-;-)
Alt rs1064796995(-;-)
Reference Rs1064796995(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49444753delC
CLNSRC
CLNACC RCV000484408.1,