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rs1085307947

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome11
Position118476863
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1085307947
dbSNP (old)rs1085307947
ClinGenrs1085307947
ebirs1085307947
HLIrs1085307947
Exacrs1085307947
Gnomadrs1085307947
Varsomers1085307947
Maprs1085307947
PheGenIrs1085307947
Biobankrs1085307947
1000 genomesrs1085307947
hgdprs1085307947
ensemblrs1085307947
gopubmedrs1085307947
geneviewrs1085307947
scholarrs1085307947
googlers1085307947
pharmgkbrs1085307947
gwascentralrs1085307947
openSNPrs1085307947
23andMers1085307947
23andMe allrs1085307947
SNPshotrs1085307947
SNPdbers1085307947
MSV3drs1085307947
GWAS Ctlgrs1085307947
Max Magnitude0
ClinVar
Risk rs1085307947(T;T)
Alt rs1085307947(T;T)
Reference Rs1085307947(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118347578G>T
CLNSRC
CLNACC RCV000489283.1,