List of variants in gene ABCC9 reported as likely benign for bone disorder

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020297.4(ABCC9):c.1848C>T (p.Asp616=)	rs61001398	0.01493
NM_020297.4(ABCC9):c.2631G>A (p.Thr877=)	rs139408145	0.00386
NM_020297.4(ABCC9):c.2093-7T>C	rs185235724	0.00261
NM_020297.4(ABCC9):c.407-14C>A	rs201279882	0.00248
NM_020297.4(ABCC9):c.2862C>T (p.Asp954=)	rs2291550	0.00041
NM_020297.4(ABCC9):c.3315+17C>T	rs200692327	0.00023
NM_020297.4(ABCC9):c.2339+13A>G	rs189255166	0.00012
NM_020297.4(ABCC9):c.142+10C>A	rs138917284	0.00007
NM_020297.4(ABCC9):c.-11T>C	rs72559432	0.00004
NM_020297.4(ABCC9):c.3462G>A (p.Arg1154=)	rs1336342134	0.00002
NM_020297.4(ABCC9):c.1671C>A (p.Thr557=)	rs746467455	0.00001
NM_020297.4(ABCC9):c.1165-6del	rs35857705
NM_020297.4(ABCC9):c.2238-17del	rs4148670
NM_020297.4(ABCC9):c.2644-11G>A	rs61926078
NM_020297.4(ABCC9):c.4450-6_4450-5del	rs4148680

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.