ClinVar Miner

List of variants in gene TSHR reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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NM_000369.2(TSHR):c.*1154dupT rs3214569
NM_000369.2(TSHR):c.1657G>A (p.Ala553Thr) rs121908872
NM_000369.2(TSHR):c.2120G>A (p.Arg707Gln) rs368452281
NM_000369.2(TSHR):c.2181G>C (p.Glu727Asp) rs1991517
NM_000369.4(TSHR):c.1206C>T (p.Ser402=)

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