List of variants in gene ACVR1 reported as likely benign for Progressive myositis ossificans

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_001111067.4(ACVR1):c.561G>A (p.Ser187=)	rs377367232	0.00007
NM_001111067.4(ACVR1):c.1395+5G>A	rs762094464	0.00004
NM_001111067.4(ACVR1):c.644-3T>C	rs745601993	0.00001

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