List of variants in gene BMPR1A reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_004329.3(BMPR1A):c.1327C>T (p.Arg443Cys)	rs35619497	0.00081
NM_004329.3(BMPR1A):c.1433G>A (p.Arg478His)	rs113849804	0.00025
NM_004329.3(BMPR1A):c.1235T>C (p.Val412Ala)	rs576247658	0.00014
NM_004329.3(BMPR1A):c.499A>G (p.Met167Val)	rs200951235	0.00007
NM_004329.3(BMPR1A):c.1401C>T (p.Tyr467=)	rs149787558	0.00004
NM_004329.3(BMPR1A):c.760C>T (p.Arg254Cys)	rs587782578	0.00004
NM_004329.3(BMPR1A):c.117C>T (p.Ser39=)	rs757333646	0.00003
NM_004329.3(BMPR1A):c.12A>G (p.Leu4=)	rs772729006	0.00002
NM_004329.3(BMPR1A):c.1368A>G (p.Pro456=)	rs864622447	0.00002
NM_004329.3(BMPR1A):c.1569G>A (p.Lys523=)	rs876659703	0.00002
NM_004329.3(BMPR1A):c.765C>T (p.Gly255=)	rs786201114	0.00002
NM_004329.3(BMPR1A):c.1362A>G (p.Gln454=)	rs764090248	0.00001
NM_004329.3(BMPR1A):c.1371T>C (p.Tyr457=)	rs1484956301	0.00001
NM_004329.3(BMPR1A):c.749T>C (p.Met250Thr)	rs587780783	0.00001
NM_004329.3(BMPR1A):c.774G>A (p.Val258=)	rs540411494	0.00001
NM_004329.3(BMPR1A):c.1101C>T (p.Asn367=)	rs863224394
NM_004329.3(BMPR1A):c.1119T>C (p.Asn373=)	rs1224219121
NM_004329.3(BMPR1A):c.117C>G (p.Ser39=)	rs757333646
NM_004329.3(BMPR1A):c.1251G>A (p.Leu417=)	rs1554891336
NM_004329.3(BMPR1A):c.195G>C (p.Gly65=)	rs765437517
NM_004329.3(BMPR1A):c.352C>T (p.Leu118=)	rs587782418
NM_004329.3(BMPR1A):c.430+10C>T	rs863224395
NM_004329.3(BMPR1A):c.953A>G (p.Tyr318Cys)	rs587778111

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