List of variants in gene DSP reported as uncertain significance 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: 83

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.273+5G>A	rs200473206	0.00031
NM_004415.4(DSP):c.2794-4dup	rs397516924	0.00023
NM_004415.4(DSP):c.6247C>T (p.Arg2083Cys)	rs370093129	0.00019
NM_004415.4(DSP):c.1949A>G (p.Asn650Ser)	rs145650440	0.00016
NM_004415.4(DSP):c.943C>T (p.Arg315Cys)	rs200476515	0.00016
NM_004415.4(DSP):c.242G>A (p.Cys81Tyr)	rs140965835	0.00014
NM_004415.4(DSP):c.521G>T (p.Cys174Phe)	rs377507763	0.00014
NM_004415.4(DSP):c.889G>A (p.Asp297Asn)	rs201930322	0.00014
NM_004415.4(DSP):c.2552T>A (p.Leu851Gln)	rs111368396	0.00013
NM_004415.4(DSP):c.3562T>C (p.Tyr1188His)	rs141508330	0.00013
NM_004415.4(DSP):c.2134G>A (p.Val712Met)	rs397516922	0.00012
NM_004415.4(DSP):c.6566G>A (p.Arg2189Gln)	rs766933370	0.00011
NM_004415.4(DSP):c.5513G>A (p.Arg1838His)	rs377715841	0.00009
NM_004415.4(DSP):c.4901G>A (p.Arg1634Gln)	rs144106775	0.00007
NM_004415.4(DSP):c.5363A>G (p.Gln1788Arg)	rs139673146	0.00007
NM_004415.4(DSP):c.8172G>T (p.Gln2724His)	rs372569211	0.00007
NM_004415.4(DSP):c.2122G>A (p.Glu708Lys)	rs773113261	0.00006
NM_004415.4(DSP):c.5197G>A (p.Asp1733Asn)	rs138588403	0.00006
NM_004415.4(DSP):c.778-20C>T	rs762596346	0.00005
NM_004415.4(DSP):c.137G>A (p.Gly46Asp)	rs140403872	0.00004
NM_004415.4(DSP):c.5795G>A (p.Arg1932His)	rs770522444	0.00004
NM_004415.4(DSP):c.8117A>T (p.Lys2706Met)	rs537588390	0.00004
NM_004415.4(DSP):c.4105G>A (p.Glu1369Lys)	rs141805096	0.00003
NM_004415.4(DSP):c.2675G>A (p.Arg892His)	rs758592774	0.00002
NM_004415.4(DSP):c.384G>A (p.Met128Ile)	rs930440897	0.00002
NM_004415.4(DSP):c.4466T>G (p.Leu1489Arg)	rs746782582	0.00002
NM_004415.4(DSP):c.4610G>A (p.Arg1537His)	rs762135558	0.00002
NM_004415.4(DSP):c.6345G>T (p.Leu2115Phe)	rs766950975	0.00002
NM_004415.4(DSP):c.6397G>A (p.Gly2133Ser)	rs372393122	0.00002
NM_004415.4(DSP):c.7924G>A (p.Val2642Ile)	rs869025397	0.00002
NM_004415.4(DSP):c.1012C>T (p.Leu338Phe)	rs774852168	0.00001
NM_004415.4(DSP):c.117G>T (p.Arg39Ser)	rs748578019	0.00001
NM_004415.4(DSP):c.1468C>T (p.Arg490Cys)	rs781084693	0.00001
NM_004415.4(DSP):c.1575-16C>G	rs756806835	0.00001
NM_004415.4(DSP):c.163G>T (p.Gly55Cys)	rs1214660308	0.00001
NM_004415.4(DSP):c.170+16G>A	rs1475829163	0.00001
NM_004415.4(DSP):c.2372T>C (p.Leu791Pro)	rs1406788095	0.00001
NM_004415.4(DSP):c.2415A>C (p.Glu805Asp)	rs1554107530	0.00001
NM_004415.4(DSP):c.2515C>T (p.His839Tyr)	rs1561693806	0.00001
NM_004415.4(DSP):c.2617C>G (p.Gln873Glu)	rs794728118	0.00001
NM_004415.4(DSP):c.3001G>T (p.Ala1001Ser)	rs1218975129	0.00001
NM_004415.4(DSP):c.308G>A (p.Arg103Gln)	rs775015862	0.00001
NM_004415.4(DSP):c.314G>A (p.Arg105Gln)	rs762238621	0.00001
NM_004415.4(DSP):c.3550C>T (p.Arg1184Trp)	rs761331634	0.00001
NM_004415.4(DSP):c.385C>T (p.Arg129Trp)	rs777763456	0.00001
NM_004415.4(DSP):c.3905G>A (p.Arg1302His)	rs760691999	0.00001
NM_004415.4(DSP):c.4112A>G (p.Asn1371Ser)	rs369649373	0.00001
NM_004415.4(DSP):c.4118C>T (p.Thr1373Ile)	rs762930286	0.00001
NM_004415.4(DSP):c.4303G>C (p.Ala1435Pro)	rs751972271	0.00001
NM_004415.4(DSP):c.4736G>A (p.Arg1579Gln)	rs397516942	0.00001
NM_004415.4(DSP):c.4754C>T (p.Ser1585Leu)	rs773622004	0.00001
NM_004415.4(DSP):c.5186T>G (p.Leu1729Arg)	rs377344768	0.00001
NM_004415.4(DSP):c.5396A>G (p.Gln1799Arg)	rs987386495	0.00001
NM_004415.4(DSP):c.5412G>T (p.Gln1804His)	rs779809935	0.00001
NM_004415.4(DSP):c.5779C>G (p.Gln1927Glu)	rs794728104	0.00001
NM_004415.4(DSP):c.5833C>T (p.Arg1945Cys)	rs1456378645	0.00001
NM_004415.4(DSP):c.5912T>C (p.Leu1971Pro)	rs397516950	0.00001
NM_004415.4(DSP):c.598-5C>T	rs765653540	0.00001
NM_004415.4(DSP):c.6038G>A (p.Arg2013Gln)	rs557263443	0.00001
NM_004415.4(DSP):c.7583A>G (p.Tyr2528Cys)	rs746932951	0.00001
NM_004415.4(DSP):c.946A>G (p.Met316Val)	rs201672777	0.00001
NM_004415.4(DSP):c.1067C>A (p.Thr356Lys)	rs780626687
NM_004415.4(DSP):c.146C>T (p.Thr49Ile)	rs151153655
NM_004415.4(DSP):c.1775G>T (p.Arg592Ile)	rs1759048949
NM_004415.4(DSP):c.1997C>T (p.Thr666Ile)	rs200053977
NM_004415.4(DSP):c.2012A>G (p.Glu671Gly)	rs758530970
NM_004415.4(DSP):c.2050G>T (p.Gly684Cys)	rs1759071281
NM_004415.4(DSP):c.2298-10C>G
NM_004415.4(DSP):c.2404G>A (p.Asp802Asn)	rs770105310
NM_004415.4(DSP):c.2631-3C>T	rs1041054817
NM_004415.4(DSP):c.2631-3_2631delinsTAGA
NM_004415.4(DSP):c.272C>T (p.Pro91Leu)	rs1561679365
NM_004415.4(DSP):c.3492C>G (p.Ile1164Met)	rs1561697488
NM_004415.4(DSP):c.3687_3689dup (p.Glu1229dup)	rs1561697838
NM_004415.4(DSP):c.3964G>A (p.Asp1322Asn)	rs1759376700
NM_004415.4(DSP):c.4232G>A (p.Arg1411Lys)
NM_004415.4(DSP):c.4717G>A (p.Val1573Met)	rs370171270
NM_004415.4(DSP):c.598-19C>G
NM_004415.4(DSP):c.6088T>C (p.Ser2030Pro)	rs1759514959
NM_004415.4(DSP):c.6160G>T (p.Ala2054Ser)	rs1759517531
NM_004415.4(DSP):c.616G>A (p.Ala206Thr)	rs794728109
NM_004415.4(DSP):c.8493_8516del (p.2827_2830SGSR[3])	rs1554109280
NM_004415.4(DSP):c.940-7T>G	rs1368622056

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.