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rs1057520177

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057520177(-;A)
Make rs1057520177(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position118503551
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1057520177
dbSNP (classic)rs1057520177
ClinGenrs1057520177
ebirs1057520177
HLIrs1057520177
Exacrs1057520177
Gnomadrs1057520177
Varsomers1057520177
LitVarrs1057520177
Maprs1057520177
PheGenIrs1057520177
Biobankrs1057520177
1000 genomesrs1057520177
hgdprs1057520177
ensemblrs1057520177
geneviewrs1057520177
scholarrs1057520177
googlers1057520177
pharmgkbrs1057520177
gwascentralrs1057520177
openSNPrs1057520177
23andMers1057520177
23andMe allrs1057520177
SNPshotrs1057520177
SNPdbers1057520177
MSV3drs1057520177
GWAS Ctlgrs1057520177
Max Magnitude0
ClinVar
Risk rs1057520177(A;A)
Alt rs1057520177(A;A)
Reference Rs1057520177(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118374266dupA
CLNSRC
CLNACC RCV000442553.1,