List of variants reported as pathogenic for Familial gestational hyperthyroidism

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000369.5(TSHR):c.1349G>A (p.Arg450His)	rs189261858	0.00023
NM_000369.5(TSHR):c.202C>T (p.Pro68Ser)	rs142063461	0.00022
NM_000369.5(TSHR):c.1515C>A (p.Ser505Arg)	rs774078708
NM_000369.5(TSHR):c.1657G>A (p.Ala553Thr)	rs121908872
NM_000369.5(TSHR):c.548A>G (p.Lys183Arg)	rs121908879

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