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rs863224889

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224889(A;A)
Make rs863224889(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position118482496
GeneKMT2A
is asnp
is mentioned by
dbSNPrs863224889
ebirs863224889
HLIrs863224889
Exacrs863224889
Varsomers863224889
Maprs863224889
PheGenIrs863224889
hapmaprs863224889
1000 genomesrs863224889
hgdprs863224889
ensemblrs863224889
gopubmedrs863224889
geneviewrs863224889
scholarrs863224889
googlers863224889
pharmgkbrs863224889
gwascentralrs863224889
openSNPrs863224889
23andMers863224889
23andMe allrs863224889
SNP Nexus

SNPshotrs863224889
SNPdbers863224889
MSV3drs863224889
GWAS Ctlgrs863224889
Max Magnitude0
ClinVar
Risk rs863224889(A;A)
Alt rs863224889(A;A)
Reference rs863224889(G;G)
Significance Probable-Pathogenic
Disease Wiedemann-Steiner syndrome
Variation info
Gene KMT2A
CLNDBN Wiedemann-Steiner syndrome
Reversed 0
HGVS NC_000011.9:g.118353211G>A
CLNSRC
CLNACC RCV000198164.1,