List of variants reported as benign for gingival disorder by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_002029.4(FPR1):c.32T>C (p.Ile11Thr)	rs5030878	0.78476
NM_002029.4(FPR1):c.301G>C (p.Val101Leu)	rs2070745	0.36919
NM_002029.4(FPR1):c.546C>A (p.Pro182=)	rs2070746	0.30428
NM_002029.4(FPR1):c.568A>T (p.Arg190Trp)	rs5030880	0.11833
NM_002029.4(FPR1):c.348C>T (p.Ile116=)	rs5030879	0.09659
NM_002029.4(FPR1):c.306T>C (p.Phe102=)	rs28930680	0.02812
NM_002029.4(FPR1):c.993C>T (p.Thr331=)	rs17849971	0.02106
NM_002029.4(FPR1):c.177C>T (p.Val59=)	rs61736491	0.01938
NM_002029.4(FPR1):c.488G>A (p.Arg163His)	rs111768566	0.00604
NM_002029.4(FPR1):c.806G>A (p.Arg269His)	rs142210016	0.00377
NM_002029.4(FPR1):c.289C>A (p.Leu97Met)	rs78488639	0.00362
NM_002029.4(FPR1):c.645C>T (p.Ser215=)	rs35264765	0.00271
NM_002029.4(FPR1):c.117C>T (p.Leu39=)	rs149382837	0.00111
NM_002029.4(FPR1):c.822C>T (p.Gly274=)	rs547725110	0.00008
NM_002029.4(FPR1):c.1037A>C (p.Glu346Ala)	rs867228
NM_002029.4(FPR1):c.1037_1038delinsCA (p.Glu346Ala)	rs1555796329
NM_002029.4(FPR1):c.576T>C (p.Asn192=)	rs1042229
NM_002029.4(FPR1):c.576T>G (p.Asn192Lys)	rs1042229

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