List of variants reported as likely pathogenic for isolated thyroid-stimulating hormone deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000549.5(TSHB):c.145G>A (p.Gly49Arg)	rs121918668	0.00001
NM_000549.5(TSHB):c.-1_5del (p.Met1_Thr2del)
NM_000549.5(TSHB):c.108_109del (p.Ala37fs)	rs2101008674
NM_000549.5(TSHB):c.230del (p.Phe77fs)	rs771834192
NM_000549.5(TSHB):c.315T>A (p.Cys105Ter)

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