ClinVar Miner

List of variants in gene combination LOC130063124, S1PR4 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003775.4(S1PR4):c.643G>A (p.Val215Ile)	rs146465201	0.00010
NM_003775.4(S1PR4):c.640G>A (p.Gly214Ser)	rs751701620	0.00006

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