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rs1057519149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519149(-;T)
Make rs1057519149(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position118473674
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1057519149
dbSNP (old)rs1057519149
ClinGenrs1057519149
ebirs1057519149
HLIrs1057519149
Exacrs1057519149
Gnomadrs1057519149
Varsomers1057519149
Maprs1057519149
PheGenIrs1057519149
Biobankrs1057519149
1000 genomesrs1057519149
hgdprs1057519149
ensemblrs1057519149
gopubmedrs1057519149
geneviewrs1057519149
scholarrs1057519149
googlers1057519149
pharmgkbrs1057519149
gwascentralrs1057519149
openSNPrs1057519149
23andMers1057519149
23andMe allrs1057519149
SNPshotrs1057519149
SNPdbers1057519149
MSV3drs1057519149
GWAS Ctlgrs1057519149
Max Magnitude0
ClinVar
Risk rs1057519149(T;T)
Alt rs1057519149(T;T)
Reference Rs1057519149(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118344389dupT
CLNSRC
CLNACC RCV000415772.1,