List of variants in gene BMP1 reported as benign for bone development disease

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006129.5(BMP1):c.2576-103C>T	rs4463424	0.99968
NM_006129.5(BMP1):c.2827-89C>T	rs11778448	0.26144
NM_006129.5(BMP1):c.2688C>T (p.Ala896=)	rs4076619	0.13111
NM_006129.5(BMP1):c.1770T>C (p.Ala590=)	rs2229777	0.11345
NM_006129.5(BMP1):c.2640C>A (p.Gly880=)	rs77242743	0.07587
NM_006129.5(BMP1):c.2155G>A (p.Val719Ile)	rs11996036	0.07088
NM_006129.5(BMP1):c.2205C>G (p.Leu735=)	rs28710878	0.03417
NM_006129.5(BMP1):c.2575+14T>C	rs28374147	0.03056
NM_006129.5(BMP1):c.1766-5C>T	rs76809016	0.02982
NM_006129.5(BMP1):c.2115C>T (p.Asp705=)	rs61729094	0.01618
NM_006129.5(BMP1):c.2450T>C (p.Val817Ala)	rs80019749	0.01155
NM_006129.5(BMP1):c.*22G>A	rs10093980	0.00767
NM_006129.5(BMP1):c.1297+14C>T	rs151163052	0.00746
NM_006129.5(BMP1):c.879C>T (p.Asn293=)	rs35120584	0.00529

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.