ClinVar Miner

List of variants reported as likely pathogenic for Familial gestational hyperthyroidism

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000369.5(TSHR):c.484C>G (p.Pro162Ala)	rs121908863	0.00010
NM_000369.5(TSHR):c.394G>C (p.Gly132Arg)	rs760874290	0.00004
NM_000369.5(TSHR):c.1192T>G (p.Cys398Gly)	rs746088246

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