"PreventionGenetics, part of Exact Sciences"[submitter] AND "S1PR2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 506084	NM_004230.4(S1PR2):c.1050C>T (p.Asn350=)	S1PR2	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1210475	NM_004230.4(S1PR2):c.919A>T (p.Arg307Trp)	S1PR2 (R307W)	Single nucleotide variant (missense variant)	S1PR2-related disorder +1 more	GLikely benign
Select item 732065	NM_004230.4(S1PR2):c.882C>T (p.Asp294=)	S1PR2	Single nucleotide variant (synonymous variant)	S1PR2-related disorder +1 more	GBenign/Likely benign
Select item 2852787	NM_004230.4(S1PR2):c.570T>C (p.Tyr190=)	S1PR2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1214728	NM_004230.4(S1PR2):c.480G>A (p.Leu160=)	S1PR2	Single nucleotide variant (synonymous variant)	S1PR2-related disorder +1 more	GBenign/Likely benign
Select item 1201244	NM_004230.4(S1PR2):c.477G>A (p.Ser159=)	S1PR2	Single nucleotide variant (synonymous variant)	S1PR2-related disorder +1 more	GBenign/Likely benign
Select item 506088	NM_004230.4(S1PR2):c.249C>T (p.Gly83=)	S1PR2	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign

ClinVar