List of variants reported as pathogenic for Farber lipogranulomatosis by OMIM

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_177924.5(ASAH1):c.107A>G (p.Tyr36Cys)	rs137853595
NM_177924.5(ASAH1):c.125+211_383-1330del
NM_177924.5(ASAH1):c.358G>C (p.Ala120Pro)	rs2117047219
NM_177924.5(ASAH1):c.413A>T (p.Glu138Val)	rs137853594
NM_177924.5(ASAH1):c.427T>G (p.Cys143Gly)	rs2117037405
NM_177924.5(ASAH1):c.505T>C (p.Trp169Arg)	rs756455049
NM_177924.5(ASAH1):c.544C>G (p.Leu182Val)	rs137853597
NM_177924.5(ASAH1):c.665C>A (p.Thr222Lys)	rs137853593
NM_177924.5(ASAH1):c.917+4A>G	rs397509415
NM_177924.5(ASAH1):c.958A>G (p.Asn320Asp)	rs137853596

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.