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rs1064796855

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position49038257
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1064796855
dbSNP (old)rs1064796855
ClinGenrs1064796855
ebirs1064796855
HLIrs1064796855
Exacrs1064796855
Gnomadrs1064796855
Varsomers1064796855
Maprs1064796855
PheGenIrs1064796855
Biobankrs1064796855
1000 genomesrs1064796855
hgdprs1064796855
ensemblrs1064796855
gopubmedrs1064796855
geneviewrs1064796855
scholarrs1064796855
googlers1064796855
pharmgkbrs1064796855
gwascentralrs1064796855
openSNPrs1064796855
23andMers1064796855
23andMe allrs1064796855
SNPshotrs1064796855
SNPdbers1064796855
MSV3drs1064796855
GWAS Ctlgrs1064796855
Max Magnitude0
ClinVar
Risk rs1064796855(-;-)
Alt rs1064796855(-;-)
Reference Rs1064796855(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49432040delG
CLNSRC
CLNACC RCV000482913.1,