List of variants in gene LAS1L reported as benign for X-linked disease

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_031206.7(LAS1L):c.1893A>C (p.Gly631=)	rs200815004	0.00022
NM_031206.7(LAS1L):c.1341A>G (p.Ala447=)	rs766767923	0.00007
NM_031206.7(LAS1L):c.1269C>T (p.Thr423=)	rs188766357	0.00005
NM_031206.7(LAS1L):c.1185G>A (p.Thr395=)	rs373278066	0.00004
NM_031206.7(LAS1L):c.707C>T (p.Thr236Met)	rs145338657	0.00003
NM_031206.7(LAS1L):c.1927+9del	rs774312008	0.00002
NM_031206.7(LAS1L):c.763C>T (p.His255Tyr)	rs1367442721	0.00001
NM_031206.7(LAS1L):c.1114G>A (p.Val372Ile)	rs186130633
NM_031206.7(LAS1L):c.1209C>G (p.Leu403=)
NM_031206.7(LAS1L):c.1301-18T>A
NM_031206.7(LAS1L):c.1788TGATGAAGA[1] (p.596DDE[1])	rs766197666
NM_031206.7(LAS1L):c.1788TGA[1] (p.Asp597del)	rs750470319
NM_031206.7(LAS1L):c.2061C>G (p.Pro687=)
NM_031206.7(LAS1L):c.362+20G>C

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