List of variants in gene ADAMTS13 reported as likely benign for not specified

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_139027.6(ADAMTS13):c.3909+32T>C	rs3094374	0.06065
NM_139027.6(ADAMTS13):c.2195C>T (p.Ala732Val)	rs41314453	0.01000
NM_139027.6(ADAMTS13):c.2494G>A (p.Val832Met)	rs34104386	0.00463
NM_139027.6(ADAMTS13):c.3171G>A (p.Ala1057=)	rs36222580	0.00268
NM_139027.6(ADAMTS13):c.1423C>T (p.Pro475Ser)	rs11575933	0.00232
NM_139027.6(ADAMTS13):c.2580C>T (p.Val860=)	rs147112200	0.00073
NM_139027.6(ADAMTS13):c.3849C>T (p.Ile1283=)	rs377686931	0.00031
NM_139027.6(ADAMTS13):c.2105-24C>G	rs886038727
NM_139027.6(ADAMTS13):c.2234+17C>A
NM_139027.6(ADAMTS13):c.3604T>C (p.Leu1202=)	rs1554796106
NM_139027.6(ADAMTS13):c.373C>A (p.Arg125=)
NM_139027.6(ADAMTS13):c.627C>G (p.Leu209=)

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