List of variants in gene BMPR1A reported as benign by Sema4, Sema4

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004329.3(BMPR1A):c.435G>A (p.Pro145=)	rs11818239	0.04296
NM_004329.3(BMPR1A):c.618A>G (p.Leu206=)	rs55992440	0.00257
NM_004329.3(BMPR1A):c.1299C>T (p.Phe433=)	rs150946485	0.00153
NM_004329.3(BMPR1A):c.1560G>A (p.Thr520=)	rs142775086	0.00120
NM_004329.3(BMPR1A):c.1395G>C (p.Pro465=)	rs55845713	0.00089
NM_004329.3(BMPR1A):c.1327C>T (p.Arg443Cys)	rs35619497	0.00081
NM_004329.3(BMPR1A):c.1243G>A (p.Glu415Lys)	rs140592056	0.00051
NM_004329.3(BMPR1A):c.676-6A>C	rs186999445	0.00014
NM_004329.3(BMPR1A):c.961C>T (p.Leu321=)	rs377412651	0.00011
NM_004329.3(BMPR1A):c.68-12A>G	rs201120747	0.00003
NM_004329.3(BMPR1A):c.1398A>C (p.Ser466=)	rs56410735	0.00001

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.