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rs1085307772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome11
Position118505025
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1085307772
dbSNP (classic)rs1085307772
ClinGenrs1085307772
ebirs1085307772
HLIrs1085307772
Exacrs1085307772
Gnomadrs1085307772
Varsomers1085307772
LitVarrs1085307772
Maprs1085307772
PheGenIrs1085307772
Biobankrs1085307772
1000 genomesrs1085307772
hgdprs1085307772
ensemblrs1085307772
geneviewrs1085307772
scholarrs1085307772
googlers1085307772
pharmgkbrs1085307772
gwascentralrs1085307772
openSNPrs1085307772
23andMers1085307772
23andMe allrs1085307772
SNPshotrs1085307772
SNPdbers1085307772
MSV3drs1085307772
GWAS Ctlgrs1085307772
Max Magnitude0
ClinVar
Risk rs1085307772(T;T)
Alt rs1085307772(T;T)
Reference Rs1085307772(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118375740C>T
CLNSRC
CLNACC RCV000489180.1,