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rs1064797056

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome11
Position118473878
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1064797056
dbSNP (old)rs1064797056
ClinGenrs1064797056
ebirs1064797056
HLIrs1064797056
Exacrs1064797056
Gnomadrs1064797056
Varsomers1064797056
Maprs1064797056
PheGenIrs1064797056
Biobankrs1064797056
1000 genomesrs1064797056
hgdprs1064797056
ensemblrs1064797056
gopubmedrs1064797056
geneviewrs1064797056
scholarrs1064797056
googlers1064797056
pharmgkbrs1064797056
gwascentralrs1064797056
openSNPrs1064797056
23andMers1064797056
23andMe allrs1064797056
SNPshotrs1064797056
SNPdbers1064797056
MSV3drs1064797056
GWAS Ctlgrs1064797056
Max Magnitude0
ClinVar
Risk rs1064797056(T;T)
Alt rs1064797056(T;T)
Reference Rs1064797056(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118344593C>T
CLNSRC
CLNACC RCV000485143.1,