Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057519744

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519744(-;CATG)
Make rs1057519744(CATG;CATG)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position171410542
GeneNPM1
is asnp
is mentioned by
dbSNPrs1057519744
dbSNP (old)rs1057519744
ClinGenrs1057519744
ebirs1057519744
HLIrs1057519744
Exacrs1057519744
Gnomadrs1057519744
Varsomers1057519744
Maprs1057519744
PheGenIrs1057519744
Biobankrs1057519744
1000 genomesrs1057519744
hgdprs1057519744
ensemblrs1057519744
gopubmedrs1057519744
geneviewrs1057519744
scholarrs1057519744
googlers1057519744
pharmgkbrs1057519744
gwascentralrs1057519744
openSNPrs1057519744
23andMers1057519744
23andMe allrs1057519744
SNPshotrs1057519744
SNPdbers1057519744
MSV3drs1057519744
GWAS Ctlgrs1057519744
Max Magnitude0
ClinVar
Risk rs1057519744(CATG;CATG) rs1057519744(CCTG;CCTG) rs1057519744(TCAG;TCAG) rs1057519744(TCTG;TCTG)
Alt rs1057519744(CATG;CATG) rs1057519744(CCTG;CCTG) rs1057519744(TCAG;TCAG) rs1057519744(TCTG;TCTG)
Reference Rs1057519744(-;-)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene NPM1
CLNDBN Acute myeloid leukemia
Reversed 0
HGVS NC_000005.9:g.170837546_170837547insCATG; NC_000005.9:g.170837546_170837547insCCTG; NC_000005.9:g.170837546_170837547insTCAG; NC_000005.9:g.170837546_170837547insTCTG
CLNSRC
CLNACC RCV000433387.1, RCV000444609.1, RCV000427692.1, RCV000437921.1,