List of variants in gene SLC34A1 reported as likely pathogenic for not provided

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_003052.5(SLC34A1):c.1223T>A (p.Val408Glu)	rs140649226	0.00011
NM_003052.5(SLC34A1):c.937-2A>C	rs754825865	0.00008
NM_003052.5(SLC34A1):c.644G>A (p.Arg215Gln)	rs1163121743	0.00005
NM_003052.5(SLC34A1):c.73C>T (p.Arg25Ter)	rs200893951	0.00004
NM_003052.5(SLC34A1):c.1006+1G>A	rs200095793	0.00001
NM_003052.5(SLC34A1):c.1007-1G>A
NM_003052.5(SLC34A1):c.109+1G>A	rs1364012682
NM_003052.5(SLC34A1):c.1174+1G>T
NM_003052.5(SLC34A1):c.1467C>A (p.Tyr489Ter)	rs1185100306
NM_003052.5(SLC34A1):c.1484G>A (p.Arg495His)
NM_003052.5(SLC34A1):c.388+2T>C
NM_003052.5(SLC34A1):c.454_480dup (p.Val152_Val160dup)	rs777543926
NM_003052.5(SLC34A1):c.458G>T (p.Gly153Val)	rs769409705
NM_003052.5(SLC34A1):c.644+42_651delinsCACCGTG
NM_003052.5(SLC34A1):c.840+2T>C

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