List of variants in gene SLC34A1 reported as benign by GeneDx

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_003052.5(SLC34A1):c.1174+253A>C	rs6420095	0.29082
NM_003052.5(SLC34A1):c.1174+179C>T	rs6556316	0.28349
NM_003052.5(SLC34A1):c.774T>C (p.His258=)	rs5030873	0.25133
NM_003052.5(SLC34A1):c.533-107G>A	rs33921462	0.21377
NM_003052.5(SLC34A1):c.389-20C>T	rs3812036	0.20052
NM_003052.5(SLC34A1):c.1175-245T>G	rs9800059	0.07610
NM_003052.5(SLC34A1):c.109+57A>G	rs73804338	0.04722
NM_003052.5(SLC34A1):c.1174+41G>T	rs6556315	0.02618
NM_003052.5(SLC34A1):c.223C>T (p.Pro75Ser)	rs61753440	0.01801
NM_003052.5(SLC34A1):c.109+29T>C	rs114460986	0.01730
NM_003052.5(SLC34A1):c.109+31G>C	rs73804337	0.01315
NM_003052.5(SLC34A1):c.1416+62C>G	rs7447593
NM_003052.5(SLC34A1):c.272_292del (p.Val91_Ala97del)	rs876661296
NM_003052.5(SLC34A1):c.532+202A>G	rs59451832

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