List of variants in gene SLC34A3 reported as likely pathogenic for bone remodeling 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001177316.2(SLC34A3):c.575C>T (p.Ser192Leu)	rs199690076	0.00059
NM_001177316.2(SLC34A3):c.1304del (p.Ser435fs)	rs771816857	0.00021
NM_001177316.2(SLC34A3):c.448+1G>A	rs150841256	0.00017
NM_001177316.2(SLC34A3):c.846G>A (p.Pro282=)	rs121918236	0.00004
NM_001177316.2(SLC34A3):c.449-1G>C	rs1345816189	0.00003
NM_001177316.2(SLC34A3):c.1242C>A (p.Tyr414Ter)	rs949841477	0.00001
NM_001177316.2(SLC34A3):c.1623G>A (p.Trp541Ter)	rs762610288	0.00001
NM_001177316.2(SLC34A3):c.448+5G>A	rs768893184	0.00001
NM_001177316.2(SLC34A3):c.846+1G>A	rs754054340	0.00001
NM_001177316.2(SLC34A3):c.1238C>A (p.Ala413Glu)	rs121918235
NM_001177316.2(SLC34A3):c.1247del (p.Leu416fs)
NM_001177316.2(SLC34A3):c.1248_1249del (p.Leu417fs)	rs757714479
NM_001177316.2(SLC34A3):c.1274C>T (p.Thr425Ile)	rs1060499697
NM_001177316.2(SLC34A3):c.1386C>G (p.Tyr462Ter)	rs777986863
NM_001177316.2(SLC34A3):c.1561dup (p.Leu521fs)	rs765816079
NM_001177316.2(SLC34A3):c.560+27_561-38del	rs746082077
NM_001177316.2(SLC34A3):c.925+20_926-48del	rs1554784044

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