ClinVar Miner

List of variants in gene LAS1L reported as uncertain significance for X-linked syndromic intellectual disability

Included ClinVar conditions (212):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_031206.4(LAS1L):c.1082C>G (p.Pro361Arg) rs867562406
NM_031206.4(LAS1L):c.1114G>C (p.Val372Leu) rs186130633
NM_031206.4(LAS1L):c.1203G>T (p.Arg401Ser) rs1569438242
NM_031206.4(LAS1L):c.1472G>A (p.Gly491Asp) rs1556301877
NM_031206.4(LAS1L):c.1705A>G (p.Lys569Glu) rs1006077682
NM_031206.4(LAS1L):c.1735G>A (p.Val579Ile) rs200862250
NM_031206.4(LAS1L):c.1892G>C (p.Gly631Ala) rs371394378
NM_031206.4(LAS1L):c.2050C>T (p.Arg684Trp) rs762602796
NM_031206.4(LAS1L):c.502G>A (p.Asp168Asn) rs1569443405
NM_031206.4(LAS1L):c.715G>T (p.Asp239Tyr) rs750436732
NM_031206.4(LAS1L):c.937G>A (p.Gly313Ser) rs745313876
NM_031206.4(LAS1L):c.940G>A (p.Val314Ile) rs137948118
NM_031206.7(LAS1L):c.1483G>A (p.Glu495Lys)
NM_031206.7(LAS1L):c.1570C>G (p.Pro524Ala)
NM_031206.7(LAS1L):c.754G>A (p.Val252Met)

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.