ClinVar Miner

List of variants in gene TSHR studied 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: 55
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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.*116G>A rs554104473
NM_000369.2(TSHR):c.*1222G>C rs2288495
NM_000369.2(TSHR):c.*125A>G rs886050855
NM_000369.2(TSHR):c.*1289A>G rs150122093
NM_000369.2(TSHR):c.*1317C>A rs886050859
NM_000369.2(TSHR):c.*137delG rs886050856
NM_000369.2(TSHR):c.*1417T>C rs2288496
NM_000369.2(TSHR):c.*1580A>G rs189084497
NM_000369.2(TSHR):c.*1620C>G rs886050860
NM_000369.2(TSHR):c.*1695T>C rs112187344
NM_000369.2(TSHR):c.*172C>A rs2268477
NM_000369.2(TSHR):c.*1742G>T rs886050861
NM_000369.2(TSHR):c.*1813T>A rs58832257
NM_000369.2(TSHR):c.*182G>T rs373305430
NM_000369.2(TSHR):c.*1898A>G rs886050862
NM_000369.2(TSHR):c.*18C>A rs77789619
NM_000369.2(TSHR):c.*1946C>T rs187891791
NM_000369.2(TSHR):c.*245C>T rs7144481
NM_000369.2(TSHR):c.*319G>A rs886050857
NM_000369.2(TSHR):c.*400T>C rs143040631
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.1191G>T (p.Val397=) rs781406064
NM_000369.2(TSHR):c.1290G>A (p.Leu430=) rs375393735
NM_000369.2(TSHR):c.1291G>A (p.Gly431Ser) rs121908883
NM_000369.2(TSHR):c.1358T>C (p.Met453Thr) rs121908864
NM_000369.2(TSHR):c.1377G>A (p.Ala459=) rs113951800
NM_000369.2(TSHR):c.1514G>A (p.Ser505Asn) rs121908876
NM_000369.2(TSHR):c.1526T>C (p.Val509Ala) rs121908874
NM_000369.2(TSHR):c.1637G>A (p.Trp546Ter) rs121908866
NM_000369.2(TSHR):c.1657G>A (p.Ala553Thr) rs121908872
NM_000369.2(TSHR):c.171-11T>C rs145265345
NM_000369.2(TSHR):c.1887G>T (p.Leu629Phe) rs121908877
NM_000369.2(TSHR):c.1891T>C (p.Phe631Leu) rs121908861
NM_000369.2(TSHR):c.1915C>T (p.Pro639Ser) rs121908880
NM_000369.2(TSHR):c.2015G>A (p.Cys672Tyr) rs121908875
NM_000369.2(TSHR):c.2120G>A (p.Arg707Gln) rs368452281
NM_000369.2(TSHR):c.2161G>T (p.Val721Phe) rs61745409
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.357T>A (p.Pro119=) rs144084915
NM_000369.2(TSHR):c.394G>C (p.Gly132Arg) rs760874290
NM_000369.2(TSHR):c.545+13A>G rs2241119
NM_000369.2(TSHR):c.548A>G (p.Lys183Arg) rs121908879
NM_000369.2(TSHR):c.561T>C (p.Asn187=) rs2075179
NM_000369.2(TSHR):c.615-6C>G rs886050854
NM_000369.2(TSHR):c.692+3G>A rs552128204
NM_000369.2(TSHR):c.842G>A (p.Ser281Asn) rs121908873
NM_000369.2(TSHR):c.881+3A>G rs186091357

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