List of variants in gene ASXL1 reported as benign by Eurofins Ntd Llc (ga)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.1954G>A (p.Gly652Ser)	rs3746609	0.00875
NM_015338.6(ASXL1):c.3692C>T (p.Ser1231Phe)	rs74638057	0.00841
NM_015338.6(ASXL1):c.3519G>A (p.Leu1173=)	rs117901891	0.00839

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