List of variants in gene S1PR2 reported as likely benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004230.4(S1PR2):c.923C>T (p.Pro308Leu)	rs200973983	0.00049
NM_004230.4(S1PR2):c.673G>A (p.Ala225Thr)	rs143046723	0.00014
NM_004230.4(S1PR2):c.729C>T (p.Ile243=)	rs148315102	0.00010
NM_004230.4(S1PR2):c.558C>T (p.Tyr186=)	rs199954220	0.00009
NM_004230.4(S1PR2):c.955G>A (p.Gly319Arg)	rs139097585	0.00004
NM_004230.4(S1PR2):c.1032C>T (p.Pro344=)	rs561751764	0.00001

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