List of variants in gene XYLT2 reported as benign for XYLT2-related disorder

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_022167.4(XYLT2):c.166G>A (p.Asp56Asn)	rs113835371	0.01001
NM_022167.4(XYLT2):c.359G>A (p.Arg120His)	rs145954495	0.00528
NM_022167.4(XYLT2):c.1581C>A (p.Pro527=)	rs377456488
NM_022167.4(XYLT2):c.2023G>A (p.Val675Met)	rs147831067

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