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rs1057518074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518074(A;A)
Make rs1057518074(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position118478096
GeneKMT2A
is asnp
is mentioned by
dbSNPrs1057518074
dbSNP (old)rs1057518074
ClinGenrs1057518074
ebirs1057518074
HLIrs1057518074
Exacrs1057518074
Gnomadrs1057518074
Varsomers1057518074
Maprs1057518074
PheGenIrs1057518074
Biobankrs1057518074
1000 genomesrs1057518074
hgdprs1057518074
ensemblrs1057518074
gopubmedrs1057518074
geneviewrs1057518074
scholarrs1057518074
googlers1057518074
pharmgkbrs1057518074
gwascentralrs1057518074
openSNPrs1057518074
23andMers1057518074
23andMe allrs1057518074
SNPshotrs1057518074
SNPdbers1057518074
MSV3drs1057518074
GWAS Ctlgrs1057518074
Max Magnitude0
ClinVar
Risk rs1057518074(A;A)
Alt rs1057518074(A;A)
Reference Rs1057518074(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KMT2A
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118348811G>A
CLNSRC
CLNACC RCV000414422.1,