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rs863224887

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224887(-;G)
Make rs863224887(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position118481731
GeneKMT2A
is asnp
is mentioned by
dbSNPrs863224887
ClinGenrs863224887
ebirs863224887
HLIrs863224887
Exacrs863224887
Varsomers863224887
Maprs863224887
PheGenIrs863224887
hapmaprs863224887
1000 genomesrs863224887
hgdprs863224887
ensemblrs863224887
gopubmedrs863224887
geneviewrs863224887
scholarrs863224887
googlers863224887
pharmgkbrs863224887
gwascentralrs863224887
openSNPrs863224887
23andMers863224887
23andMe allrs863224887
SNP Nexus

SNPshotrs863224887
SNPdbers863224887
MSV3drs863224887
GWAS Ctlgrs863224887
Max Magnitude0
ClinVar
Risk rs863224887(G;G)
Alt rs863224887(G;G)
Reference Rs863224887(;)
Significance Pathogenic
Disease Wiedemann-Steiner syndrome
Variation info
Gene KMT2A
CLNDBN Wiedemann-Steiner syndrome
Reversed 0
HGVS NC_000011.9:g.118352446dupG
CLNSRC
CLNACC RCV000199889.1,