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rs1064793649

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position49053606
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1064793649
dbSNP (old)rs1064793649
ClinGenrs1064793649
ebirs1064793649
HLIrs1064793649
Exacrs1064793649
Gnomadrs1064793649
Varsomers1064793649
LitVarrs1064793649
Maprs1064793649
PheGenIrs1064793649
Biobankrs1064793649
1000 genomesrs1064793649
hgdprs1064793649
ensemblrs1064793649
gopubmedrs1064793649
geneviewrs1064793649
scholarrs1064793649
googlers1064793649
pharmgkbrs1064793649
gwascentralrs1064793649
openSNPrs1064793649
23andMers1064793649
23andMe allrs1064793649
SNPshotrs1064793649
SNPdbers1064793649
MSV3drs1064793649
GWAS Ctlgrs1064793649
Max Magnitude0
ClinVar
Risk rs1064793649(-;-)
Alt rs1064793649(-;-)
Reference Rs1064793649(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49447389delC
CLNSRC
CLNACC RCV000486792.1,