List of variants in gene ASXL1 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.3306G>T (p.Glu1102Asp)	rs139115934	0.00916
NM_015338.6(ASXL1):c.3513G>A (p.Arg1171=)	rs150391716	0.00538
NM_015338.6(ASXL1):c.3745A>G (p.Met1249Val)	rs146141075	0.00205
NM_015338.6(ASXL1):c.2957A>G (p.Asn986Ser)	rs145132837	0.00178
NM_015338.6(ASXL1):c.4189G>A (p.Gly1397Ser)	rs146464648	0.00113
NM_015338.6(ASXL1):c.1520T>A (p.Ile507Asn)	rs138971201	0.00079
NM_015338.6(ASXL1):c.-88GCC[5]	rs886056593
NM_015338.6(ASXL1):c.1465C>G (p.Arg489Gly)	rs142172134
NM_015338.6(ASXL1):c.2110G>A (p.Gly704Arg)	rs151317625

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