List of variants in gene S1PR2 reported by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
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.333T>C (p.Ser111=)	rs745577083	0.00036
NM_004230.4(S1PR2):c.981A>G (p.Pro327=)	rs146709827	0.00008
NM_004230.4(S1PR2):c.632G>A (p.Arg211His)	rs141230424	0.00007
NM_004230.4(S1PR2):c.986G>A (p.Arg329His)	rs143246348	0.00004
NM_004230.4(S1PR2):c.486C>T (p.Leu162=)	rs375693128	0.00001
NM_004230.4(S1PR2):c.985C>T (p.Arg329Cys)	rs765378016	0.00001
NM_004230.4(S1PR2):c.744C>A (p.Pro248=)	rs141379245

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