List of variants in gene SLC34A1 reported as benign for Hypercalcemia, infantile, 2

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003052.5(SLC34A1):c.774T>C (p.His258=)	rs5030873	0.25133
NM_003052.5(SLC34A1):c.389-20C>T	rs3812036	0.20052
NM_003052.5(SLC34A1):c.272_292del (p.Val91_Ala97del)	rs876661296

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