List of variants in gene FLVCR2 reported as benign for Fowler syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_017791.3(FLVCR2):c.648C>G (p.Ser216=)	rs2287017	0.37676
NM_017791.3(FLVCR2):c.47T>C (p.Val16Ala)	rs2287015	0.37478
NM_017791.2(FLVCR2):c.-356G>C	rs3813550	0.11387
NM_017791.3(FLVCR2):c.-121CT[1]	rs1322268460
NM_017791.3(FLVCR2):c.543G>A (p.Val181=)	rs2287016

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