List of variants in gene combination LOC130058566, XYLT1 reported as likely benign for bone disorder

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_022166.4(XYLT1):c.421C>T (p.Arg141Trp)	rs74993523	0.00252
NM_022166.4(XYLT1):c.546G>A (p.Ala182=)	rs144423897	0.00015
NM_022166.4(XYLT1):c.541T>C (p.Leu181=)	rs148434592	0.00007
NM_022166.4(XYLT1):c.558G>A (p.Pro186=)	rs538937903	0.00003
NM_022166.4(XYLT1):c.403-18C>T	rs767635029	0.00001
NM_022166.4(XYLT1):c.504C>T (p.Phe168=)	rs1279570396	0.00001
NM_022166.4(XYLT1):c.537T>C (p.Pro179=)	rs781173341	0.00001
NM_022166.4(XYLT1):c.403-9C>G
NM_022166.4(XYLT1):c.456C>T (p.Asn152=)
NM_022166.4(XYLT1):c.570G>A (p.Lys190=)	rs2506675653

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