List of variants in gene CEP128, TSHR studied for hypothyroidism, congenital, nongoitrous

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000369.5(TSHR):c.154C>A (p.Pro52Thr)	rs2234919	0.04384
NM_000369.5(TSHR):c.106G>C (p.Asp36His)	rs61747482	0.00505
NM_000369.5(TSHR):c.-60G>A	rs201252762	0.00031
NM_000369.5(TSHR):c.100G>A (p.Glu34Lys)	rs45499704	0.00025
NM_000369.5(TSHR):c.157A>C (p.Ser53Arg)	rs886050853	0.00003
NM_000369.2(TSHR):c.-166C>T	rs1180169266	0.00001
NM_000369.5(TSHR):c.122G>C (p.Cys41Ser)	rs121908869	0.00001
NM_000369.5(TSHR):c.170T>C (p.Leu57Pro)	rs200401152	0.00001
NM_000369.2(TSHR):c.-102C>T	rs1886616129

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