List of variants in gene combination PSMC2, SLC26A5 reported as uncertain significance

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002803.4(PSMC2):c.119C>G (p.Thr40Ser)	rs376614496	0.00002
NM_002803.4(PSMC2):c.1031G>A (p.Ser344Asn)	rs372290123	0.00001
NM_002803.4(PSMC2):c.154A>T (p.Ile52Phe)	rs1352254476	0.00001
NM_002803.4(PSMC2):c.187A>G (p.Thr63Ala)	rs1819947502	0.00001
NM_002803.4(PSMC2):c.1041T>A (p.Asp347Glu)
NM_002803.4(PSMC2):c.1078C>T (p.Arg360Cys)
NM_002803.4(PSMC2):c.1124G>A (p.Arg375Gln)
NM_002803.4(PSMC2):c.1234G>T (p.Ala412Ser)
NM_002803.4(PSMC2):c.302T>C (p.Ile101Thr)	rs2485107058
NM_002803.4(PSMC2):c.325C>T (p.Pro109Ser)	rs1820441024
NM_002803.4(PSMC2):c.704C>T (p.Ala235Val)
NM_002803.4(PSMC2):c.751G>T (p.Gly251Cys)	rs1820573027
NM_206883.3(SLC26A5):c.2042-9101dup	rs2116226653

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.