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rs1064797162

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position118476841
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1064797162
dbSNP (old)rs1064797162
ClinGenrs1064797162
ebirs1064797162
HLIrs1064797162
Exacrs1064797162
Gnomadrs1064797162
Varsomers1064797162
Maprs1064797162
PheGenIrs1064797162
Biobankrs1064797162
1000 genomesrs1064797162
hgdprs1064797162
ensemblrs1064797162
gopubmedrs1064797162
geneviewrs1064797162
scholarrs1064797162
googlers1064797162
pharmgkbrs1064797162
gwascentralrs1064797162
openSNPrs1064797162
23andMers1064797162
23andMe allrs1064797162
SNPshotrs1064797162
SNPdbers1064797162
MSV3drs1064797162
GWAS Ctlgrs1064797162
Max Magnitude0
ClinVar
Risk rs1064797162(T;T)
Alt rs1064797162(T;T)
Reference Rs1064797162(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118347556G>T
CLNSRC
CLNACC RCV000487778.1,