List of variants in gene FRMPD4 reported as uncertain significance by Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001368397.1(FRMPD4):c.3889G>C (p.Ala1297Pro)	rs754514737	0.00002
NM_001368397.1(FRMPD4):c.1778G>A (p.Arg593Gln)	rs2042078311	0.00001
NM_001368397.1(FRMPD4):c.1537C>T (p.Arg513Trp)	rs1602359193
NM_001368397.1(FRMPD4):c.3640C>G (p.Gln1214Glu)	rs2519867999
NM_001368397.1(FRMPD4):c.4562G>A (p.Arg1521Lys)	rs947906329
NM_001368397.1(FRMPD4):c.474C>A (p.Pro158=)	rs147360584
NM_001368397.1(FRMPD4):c.5022G>A (p.Met1674Ile)	rs1260187604
NM_001368397.1(FRMPD4):c.681+504C>A	rs906030491

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