List of variants in gene S1PR2 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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: 14

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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.480G>A (p.Leu160=)	rs144510483	0.00127
NM_004230.4(S1PR2):c.717A>G (p.Leu239=)	rs150395684	0.00078
NM_004230.4(S1PR2):c.882C>T (p.Asp294=)	rs35493500	0.00044
NM_004230.4(S1PR2):c.477G>A (p.Ser159=)	rs200965528	0.00016
NM_004230.4(S1PR2):c.855C>T (p.Pro285=)	rs202092003	0.00006
NM_004230.4(S1PR2):c.844C>T (p.Leu282=)	rs186708543	0.00004
NM_004230.4(S1PR2):c.919A>C (p.Arg307=)	rs2116942

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