"PreventionGenetics, part of Exact Sciences"[submitter] AND "SFRP4"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1332946	NM_003014.4(SFRP4):c.1019G>A (p.Arg340Lys)	SFRP4 (R340K)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1287094	NM_003014.4(SFRP4):c.958C>A (p.Pro320Thr)	SFRP4 (P320T)	Single nucleotide variant (missense variant)	SFRP4-related disorder +2 more	GBenign
Select item 1600043	NM_003014.4(SFRP4):c.915C>T (p.Ala305=)	SFRP4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1332947	NM_003014.4(SFRP4):c.786C>T (p.Arg262=)	SFRP4	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1332948	NM_003014.4(SFRP4):c.567G>A (p.Thr189=)	SFRP4	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1534744	NM_003014.4(SFRP4):c.24G>A (p.Ala8=)	SFRP4	Single nucleotide variant (synonymous variant)	SFRP4-related disorder +1 more	GLikely benign

ClinVar