"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "FSHR"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1675781	NM_000145.4(FSHR):c.1683C>T (p.Ile561=)	FSHR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3027273	NM_000145.4(FSHR):c.1365G>C (p.Leu455=)	FSHR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 336482	NM_000145.4(FSHR):c.1330G>A (p.Ala444Thr)	FSHR (A444T +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2311847	NM_000145.4(FSHR):c.1073A>T (p.Asp358Val)	FSHR (D332V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2571079	NM_000145.4(FSHR):c.854+5G>A	FSHR	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 336489	NM_000145.4(FSHR):c.485G>A (p.Arg162Lys)	FSHR (R162K)	Single nucleotide variant (missense variant +1 more)	FSHR-related condition +3 more	GConflicting classifications of pathogenicity
Select item 2650900	NM_000145.4(FSHR):c.374+2783T>C	FSHR	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2672813	NM_000145.4(FSHR):c.3G>A (p.Met1Ile)	FSHR (M1I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

ClinVar