ClinVar Miner

List of variants in gene combination MFSD11, SRSF2 reported as likely pathogenic for bone marrow neoplasm

Included ClinVar conditions (61):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001195427.2(SRSF2):c.284C>G (p.Pro95Arg) rs751713049

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