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rs1057519745

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519745(-;TGTACGGT)
Make rs1057519745(TGTACGGT;TGTACGGT)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position32396363
GeneWT1
is asnp
is mentioned by
dbSNPrs1057519745
dbSNP (classic)rs1057519745
ClinGenrs1057519745
ebirs1057519745
HLIrs1057519745
Exacrs1057519745
Gnomadrs1057519745
Varsomers1057519745
LitVarrs1057519745
Maprs1057519745
PheGenIrs1057519745
Biobankrs1057519745
1000 genomesrs1057519745
hgdprs1057519745
ensemblrs1057519745
geneviewrs1057519745
scholarrs1057519745
googlers1057519745
pharmgkbrs1057519745
gwascentralrs1057519745
openSNPrs1057519745
23andMers1057519745
23andMe allrs1057519745
SNPshotrs1057519745
SNPdbers1057519745
MSV3drs1057519745
GWAS Ctlgrs1057519745
Max Magnitude0
ClinVar
Risk rs1057519745(TGTACGGT;TGTACGGT)
Alt rs1057519745(TGTACGGT;TGTACGGT)
Reference Rs1057519745(-;-)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene WT1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000011.9:g.32417909_32417910insACCGTACA
CLNSRC
CLNACC RCV000418995.1,