ClinVar Miner

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

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_000369.2(TSHR):c.*1106G>T rs150923034
NM_000369.2(TSHR):c.*1152T>A rs2288494
NM_000369.2(TSHR):c.*1154dupT rs3214569
NM_000369.2(TSHR):c.*1222G>C rs2288495
NM_000369.2(TSHR):c.*1289A>G rs150122093
NM_000369.2(TSHR):c.*1417T>C rs2288496
NM_000369.2(TSHR):c.*1580A>G rs189084497
NM_000369.2(TSHR):c.*172C>A rs2268477
NM_000369.2(TSHR):c.*1813T>A rs58832257
NM_000369.2(TSHR):c.*182G>T rs373305430
NM_000369.2(TSHR):c.*18C>A rs77789619
NM_000369.2(TSHR):c.*245C>T rs7144481
NM_000369.2(TSHR):c.*431T>C rs17630128
NM_000369.2(TSHR):c.*474G>T rs61266735
NM_000369.2(TSHR):c.*728A>G rs73342245
NM_000369.2(TSHR):c.*909C>T rs2288493
NM_000369.2(TSHR):c.*960T>C rs142517342
NM_000369.2(TSHR):c.1377G>A (p.Ala459=) rs113951800
NM_000369.2(TSHR):c.1657G>A (p.Ala553Thr) rs121908872
NM_000369.2(TSHR):c.2181G>C (p.Glu727Asp) rs1991517
NM_000369.2(TSHR):c.2232C>G (p.Asn744Lys) rs61743974
NM_000369.2(TSHR):c.545+13A>G rs2241119
NM_000369.2(TSHR):c.561T>C (p.Asn187=) rs2075179
NM_000369.2(TSHR):c.881+3A>G rs186091357

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