List of variants reported as likely benign for McKusick-Kaufman syndrome by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_170784.3(MKKS):c.15A>G (p.Glu5=)	rs145396188	0.00074
NM_170784.3(MKKS):c.231G>A (p.Leu77=)	rs373913834	0.00035
NM_170784.3(MKKS):c.416G>A (p.Arg139Gln)	rs145045986	0.00031
NM_170784.3(MKKS):c.1356T>C (p.Ser452=)	rs201977053	0.00008
NM_170784.3(MKKS):c.822C>T (p.Asp274=)	rs761342904	0.00003
NM_170784.3(MKKS):c.1360C>T (p.Leu454=)	rs1210784201	0.00001
NM_170784.3(MKKS):c.1695T>C (p.Val565=)	rs554395344	0.00001
NM_170784.3(MKKS):c.210A>C (p.Thr70=)	rs1471154105	0.00001
NM_170784.3(MKKS):c.1162-12del	rs781066396
NM_170784.3(MKKS):c.207C>T (p.Val69=)	rs1382659817
NM_170784.3(MKKS):c.717C>T (p.Leu239=)	rs1214711344

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.