List of variants in gene SLC35D1 reported as benign for bone development disease

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_015139.3(SLC35D1):c.636+45C>A	rs1024229	0.68971
NM_015139.3(SLC35D1):c.636+28T>G	rs1024230	0.68966
NM_015139.3(SLC35D1):c.729+5G>C	rs7539628	0.07175
NM_015139.3(SLC35D1):c.730-8T>C	rs138429988	0.00215
NM_015139.3(SLC35D1):c.672A>C (p.Ala224=)	rs138369664	0.00111
NM_015139.3(SLC35D1):c.203+12G>T	rs200679737	0.00047
NM_015139.3(SLC35D1):c.797+16C>T	rs374531477	0.00009
NM_015139.3(SLC35D1):c.244G>A (p.Ala82Thr)	rs10157422
NM_015139.3(SLC35D1):c.393-3del	rs199880356
NM_015139.3(SLC35D1):c.393-5del	rs5774854
NM_015139.3(SLC35D1):c.393-5dup	rs5774854

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