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rs864309569

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309569(C;G)
Make rs864309569(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position118501681
GeneKMT2A
is asnp
is mentioned by
dbSNPrs864309569
ebirs864309569
HLIrs864309569
Exacrs864309569
Varsomers864309569
Maprs864309569
PheGenIrs864309569
hapmaprs864309569
1000 genomesrs864309569
hgdprs864309569
ensemblrs864309569
gopubmedrs864309569
geneviewrs864309569
scholarrs864309569
googlers864309569
pharmgkbrs864309569
gwascentralrs864309569
openSNPrs864309569
23andMers864309569
23andMe allrs864309569
SNP Nexus

SNPshotrs864309569
SNPdbers864309569
MSV3drs864309569
GWAS Ctlgrs864309569
Max Magnitude0
ClinVar
Risk rs864309569(G;G)
Alt rs864309569(G;G)
Reference rs864309569(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118372396C>G
CLNSRC
CLNACC RCV000203050.1,