ClinVar Miner

List of variants in gene LAS1L reported as likely benign for X-linked syndromic intellectual disability

Included ClinVar conditions (165):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_031206.4(LAS1L):c.1371C>T (p.Ser457=) rs761061736
NM_031206.4(LAS1L):c.159G>A (p.Gln53=) rs144560954
NM_031206.4(LAS1L):c.1691T>C (p.Val564Ala) rs148989578
NM_031206.4(LAS1L):c.381A>G (p.Ser127=) rs992864125
NM_031206.4(LAS1L):c.747C>T (p.Ser249=) rs745356580
NM_031206.4(LAS1L):c.99G>C (p.Ser33=) rs779407196

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