ClinVar Miner

List of variants reported as pathogenic for amyloidosis, primary localized cutaneous, 3

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002510.3(GPNMB):c.565C>T (p.Arg189Ter) rs140352180 0.00016
NM_002510.3(GPNMB):c.1056del (p.Pro353fs) rs763065333
NM_002510.3(GPNMB):c.1118-2A>G
NM_002510.3(GPNMB):c.296del (p.Asn99fs) rs1554300664
NM_002510.3(GPNMB):c.660T>G (p.Tyr220Ter) rs770211260
NM_002510.3(GPNMB):c.719_720del (p.Val240fs) rs747723062
NM_002510.3(GPNMB):c.877_880del (p.Val293fs) rs773435101

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.