List of variants reported as likely pathogenic for anemia by Database of Curated Mutations (DoCM)

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		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004972.4(JAK2):c.1849G>T (p.Val617Phe)	rs77375493	0.00036
NM_005373.3(MPL):c.1514G>A (p.Ser505Asn)	rs121913614

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