ClinVar Miner

List of variants in gene S1PR2 reported as benign by Athena Diagnostics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004230.4(S1PR2):c.1050C>T (p.Asn350=)	rs116191851	0.02875
NM_004230.4(S1PR2):c.857T>C (p.Val286Ala)	rs117064827	0.00650

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