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rs1057520696

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057520696(A;A)
Make rs1057520696(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position118504462
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1057520696
dbSNP (old)rs1057520696
ClinGenrs1057520696
ebirs1057520696
HLIrs1057520696
Exacrs1057520696
Gnomadrs1057520696
Varsomers1057520696
Maprs1057520696
PheGenIrs1057520696
Biobankrs1057520696
1000 genomesrs1057520696
hgdprs1057520696
ensemblrs1057520696
gopubmedrs1057520696
geneviewrs1057520696
scholarrs1057520696
googlers1057520696
pharmgkbrs1057520696
gwascentralrs1057520696
openSNPrs1057520696
23andMers1057520696
23andMe allrs1057520696
SNPshotrs1057520696
SNPdbers1057520696
MSV3drs1057520696
GWAS Ctlgrs1057520696
Max Magnitude0
ClinVar
Risk rs1057520696(A;A)
Alt rs1057520696(A;A)
Reference Rs1057520696(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118375177T>A
CLNSRC
CLNACC RCV000442703.1,