List of variants in gene XYLT1 reported as benign for bone development disease

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_022166.4(XYLT1):c.2028-37A>C	rs3812961	0.34884
NM_022166.4(XYLT1):c.2675G>A (p.Arg892Gln)	rs35309694	0.09774
NM_022166.4(XYLT1):c.2655C>T (p.Pro885=)	rs924260	0.07855
NM_022166.4(XYLT1):c.2515G>A (p.Val839Ile)	rs7200466	0.06145
NM_022166.4(XYLT1):c.2224-12C>T	rs12325442	0.06125
NM_022166.4(XYLT1):c.668C>G (p.Ala223Gly)	rs113276942	0.04995
NM_022166.4(XYLT1):c.343G>T (p.Ala115Ser)	rs61758388	0.01927
NM_022166.4(XYLT1):c.1077C>T (p.His359=)	rs35488326	0.01851
NM_022166.4(XYLT1):c.913+9C>T	rs79173410	0.01688
NM_022166.4(XYLT1):c.606A>G (p.Lys202=)	rs114030556	0.00708
NM_022166.4(XYLT1):c.2370C>A (p.Val790=)	rs74750647	0.00372
NM_022166.4(XYLT1):c.2226C>T (p.Val742=)	rs139693964	0.00304
NM_022166.4(XYLT1):c.363+18C>G	rs367589791	0.00225
NM_022166.4(XYLT1):c.2028-15C>T	rs150179077	0.00203
NM_022166.4(XYLT1):c.2296C>G (p.Pro766Ala)	rs12325439	0.00051
NM_022166.4(XYLT1):c.1272G>A (p.Ala424=)	rs144531370	0.00031
NM_022166.4(XYLT1):c.657C>T (p.Pro219=)	rs146043560	0.00026
NM_022166.4(XYLT1):c.2358T>C (p.Asp786=)	rs145615486	0.00024
NM_022166.4(XYLT1):c.2656G>T (p.Ala886Ser)	rs143481827	0.00019
NM_022166.4(XYLT1):c.951C>T (p.Ser317=)	rs145318002	0.00017
NM_022166.4(XYLT1):c.1044C>T (p.Ala348=)	rs372015293	0.00011
NM_022166.4(XYLT1):c.1289+13A>G	rs759329282	0.00010
NM_022166.4(XYLT1):c.624C>T (p.Phe208=)	rs372923585	0.00001
NM_022166.4(XYLT1):c.1086+44G>A	rs11075341
NM_022166.4(XYLT1):c.1284C>G (p.Pro428=)	rs28709752
NM_022166.4(XYLT1):c.2028-16G>C
NM_022166.4(XYLT1):c.2331T>C (p.Asn777=)	rs7201590
NM_022166.4(XYLT1):c.2631C>T (p.Pro877=)	rs34511974
NM_022166.4(XYLT1):c.366T>C (p.Asp122=)
NM_022166.4(XYLT1):c.402+18C>T	rs111904908
NM_022166.4(XYLT1):c.630G>A (p.Gly210=)
NM_022166.4(XYLT1):c.913+15del	rs2141757493

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