List of variants in gene S1PR2 reported as uncertain significance 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004230.4(S1PR2):c.632G>A (p.Arg211His)	rs141230424	0.00007
NM_004230.4(S1PR2):c.985C>T (p.Arg329Cys)	rs765378016	0.00002
NM_004230.4(S1PR2):c.986G>A (p.Arg329His)

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