List of variants in gene FOXL2 reported as not provided

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_023067.4(FOXL2):c.1045C>G (p.Arg349Gly)	rs201840174	0.00013
NM_023067.4(FOXL2):c.560G>A (p.Gly187Asp)	rs121908359	0.00001
NM_023067.4(FOXL2):c.402C>G (p.Cys134Trp)	rs1057519865
NM_023067.4(FOXL2):c.650C>T (p.Ser217Phe)	rs797044527
NM_023067.4(FOXL2):c.655C>T (p.Gln219Ter)	rs104893741
NM_023067.4(FOXL2):c.804dup (p.Gly269fs)	rs797044528
NM_023067.4(FOXL2):c.841_857dup (p.Pro287fs)	rs797044529
NM_023067.4(FOXL2):c.843_859dup (p.Pro287fs)	rs672601359
NM_023067.4(FOXL2):c.843_865dup (p.His289fs)	rs797044530
NM_023067.4(FOXL2):c.854del (p.Pro285fs)	rs797044531
NM_023067.4(FOXL2):c.855_871del (p.Pro287fs)	rs797044532
NM_023067.4(FOXL2):c.855_871dup (p.His291fs)	rs797044532

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