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rs1064797168

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Chromosome12
Position49046682
GeneKMT2D
is asnp
is mentioned by
dbSNPrs1064797168
dbSNP (old)rs1064797168
ClinGenrs1064797168
ebirs1064797168
HLIrs1064797168
Exacrs1064797168
Gnomadrs1064797168
Varsomers1064797168
Maprs1064797168
PheGenIrs1064797168
Biobankrs1064797168
1000 genomesrs1064797168
hgdprs1064797168
ensemblrs1064797168
gopubmedrs1064797168
geneviewrs1064797168
scholarrs1064797168
googlers1064797168
pharmgkbrs1064797168
gwascentralrs1064797168
openSNPrs1064797168
23andMers1064797168
23andMe allrs1064797168
SNPshotrs1064797168
SNPdbers1064797168
MSV3drs1064797168
GWAS Ctlgrs1064797168
Max Magnitude0
ClinVar
Risk rs1064797168(-;-)
Alt rs1064797168(-;-)
Reference Rs1064797168(TG;TG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2D
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.49440465_49440466delCA
CLNSRC
CLNACC RCV000487709.1,