List of variants in gene ASXL1 reported as likely pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.2036dup (p.Gly680fs)	rs1600586587
NM_015338.6(ASXL1):c.2068_2069del (p.Asp690fs)
NM_015338.6(ASXL1):c.3747_3748del (p.Met1249fs)
NM_015338.6(ASXL1):c.4127dup (p.Pro1377fs)	rs1555912897

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