List of variants in gene FLCN studied for reproductive system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.1133G>A (p.Ser378Asn)	rs769489773	0.00002
NM_144997.7(FLCN):c.502C>T (p.Arg168Cys)	rs587778367	0.00001
NM_144997.7(FLCN):c.562T>A (p.Phe188Ile)	rs1407566775	0.00001
NM_144997.7(FLCN):c.1085G>T (p.Arg362Leu)	rs559055296
NM_144997.7(FLCN):c.1141G>A (p.Val381Met)	rs1347669124
NM_144997.7(FLCN):c.1283C>G (p.Pro428Arg)	rs199889477
NM_144997.7(FLCN):c.1306G>A (p.Ala436Thr)	rs2144840565
NM_144997.7(FLCN):c.1428C>A (p.Asp476Glu)
NM_144997.7(FLCN):c.319G>A (p.Val107Ile)	rs1372666497
NM_144997.7(FLCN):c.437A>T (p.Glu146Val)
NM_144997.7(FLCN):c.538A>C (p.Ile180Leu)
NM_144997.7(FLCN):c.754G>T (p.Ala252Ser)

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