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Gene: FSHR & Disease: Twinning, Dizygotic, 4 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
812692	FSHR	c.1121T>A	p.Ile374Asn (p.I374N)	NM_000145.4 M	SNV	VUS	1 +	0
16246	FSHR	c.919G>A	p.Ala307Thr (p.A307T)	NM_000145.4 M	SNV	B	4 +	0
812692	FSHR	c.1043T>A	p.Ile348Asn (p.I348N)	NM_181446.3	SNV	VUS	1 +	0
16246	FSHR	c.841G>A	p.Ala281Thr (p.A281T)	NM_181446.3	SNV	B	4 +	0

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