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rs762890562

From SNPedia

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,