List of variants in gene ASXL1 reported as likely benign for Bohring-Opitz syndrome

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_015338.6(ASXL1):c.2618C>T (p.Pro873Leu)	rs202098158	0.00006
NM_015338.6(ASXL1):c.1463C>T (p.Ser488Phe)	rs781545960	0.00005
NM_015338.6(ASXL1):c.2802T>C (p.Ala934=)	rs571165637	0.00005
NM_015338.6(ASXL1):c.1698G>C (p.Glu566Asp)	rs1279708959	0.00001
NM_015338.6(ASXL1):c.3212C>T (p.Ala1071Val)	rs531415735	0.00001
NM_015338.6(ASXL1):c.2544A>T (p.Thr848=)	rs142836262
NM_015338.6(ASXL1):c.3965C>G (p.Pro1322Arg)	rs141930107

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