List of variants in gene S1PR2 reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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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.642C>T (p.Cys214=)	rs79482117	0.01396
NM_004230.4(S1PR2):c.30C>A (p.Asn10Lys)	rs56357614	0.00821
NM_004230.4(S1PR2):c.857T>C (p.Val286Ala)	rs117064827	0.00650
NM_004230.4(S1PR2):c.903G>A (p.Arg301=)	rs149865919	0.00506
NM_004230.4(S1PR2):c.672C>T (p.Ala224=)	rs73922356	0.00358
NM_004230.4(S1PR2):c.249C>T (p.Gly83=)	rs73922357	0.00331
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.781G>A (p.Val261Ile)	rs199824841	0.00003
NM_004230.4(S1PR2):c.1032C>T (p.Pro344=)	rs561751764	0.00001
NM_004230.4(S1PR2):c.878G>A (p.Arg293Gln)	rs376403797	0.00001
NM_004230.4(S1PR2):c.919A>C (p.Arg307=)	rs2116942

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