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rs762890562

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs762890562(-;CTAC)
Make rs762890562(CTAC;CTAC)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position177515944
GeneDDX41
is asnp
is mentioned by
dbSNPrs762890562
ClinGenrs762890562
ebirs762890562
HLIrs762890562
Exacrs762890562
Varsomers762890562
Maprs762890562
PheGenIrs762890562
hapmaprs762890562
1000 genomesrs762890562
hgdprs762890562
ensemblrs762890562
gopubmedrs762890562
geneviewrs762890562
scholarrs762890562
googlers762890562
pharmgkbrs762890562
gwascentralrs762890562
openSNPrs762890562
23andMers762890562
23andMe allrs762890562
SNP Nexus

SNPshotrs762890562
SNPdbers762890562
MSV3drs762890562
GWAS Ctlgrs762890562
Max Magnitude0
ClinVar
Risk rs762890562(CATC;CATC)
Alt rs762890562(CATC;CATC)
Reference Rs762890562(-;-)
Significance Other
Disease Acute myeloid leukemia Myeloproliferative/lymphoproliferative neoplasms
Variation info
Gene DDX41
CLNDBN Acute myeloid leukemia Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to
Reversed 0
HGVS NC_000005.9:g.176942946_176942949dupCATC
CLNSRC OMIM Allelic Variant
CLNACC RCV000193600.1, RCV000210272.1,