ClinVar Miner

List of variants in gene GHSR studied for adrenal gland disease

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_198407.2(GHSR):c.*1024G>C rs9880206
NM_198407.2(GHSR):c.*1046T>A rs756728640
NM_198407.2(GHSR):c.*1109G>T rs562416
NM_198407.2(GHSR):c.*114A>G rs477251
NM_198407.2(GHSR):c.*122C>T rs482204
NM_198407.2(GHSR):c.*1268T>C rs755925335
NM_198407.2(GHSR):c.*1308T>G rs73039028
NM_198407.2(GHSR):c.*1345G>T rs886058181
NM_198407.2(GHSR):c.*1506C>A rs886058180
NM_198407.2(GHSR):c.*1554C>T rs754352155
NM_198407.2(GHSR):c.*1608C>T rs886058179
NM_198407.2(GHSR):c.*1676_*1679del rs150657222
NM_198407.2(GHSR):c.*1815C>G rs762604209
NM_198407.2(GHSR):c.*1832G>A rs886058178
NM_198407.2(GHSR):c.*1880delA rs5854471
NM_198407.2(GHSR):c.*294C>A rs543920867
NM_198407.2(GHSR):c.*300G>A rs886058185
NM_198407.2(GHSR):c.*472C>T rs886058184
NM_198407.2(GHSR):c.*561_*568del rs146582211
NM_198407.2(GHSR):c.*758G>A rs886058183
NM_198407.2(GHSR):c.*792G>C rs9880652
NM_198407.2(GHSR):c.*796A>T rs58550930
NM_198407.2(GHSR):c.*813A>G rs147683685
NM_198407.2(GHSR):c.*829C>A rs535110477
NM_198407.2(GHSR):c.*834C>A rs565105
NM_198407.2(GHSR):c.*842T>A rs886058182
NM_198407.2(GHSR):c.-23G>A rs200645708
NM_198407.2(GHSR):c.1017A>G (p.Gly339=) rs138507814
NM_198407.2(GHSR):c.1051C>T (p.Leu351=) rs777016625
NM_198407.2(GHSR):c.171C>T (p.Gly57=) rs495225
NM_198407.2(GHSR):c.271C>T (p.Leu91Phe) rs79053943
NM_198407.2(GHSR):c.447C>G (p.Leu149=) rs2232169
NM_198407.2(GHSR):c.477G>A (p.Arg159=) rs572169
NM_198407.2(GHSR):c.60C>T (p.Asp20=) rs2232165
NM_198407.2(GHSR):c.611C>A (p.Ala204Glu) rs121917883
NM_198407.2(GHSR):c.6G>A (p.Trp2Ter) rs267606843
NM_198407.2(GHSR):c.709A>T (p.Arg237Trp) rs199588904
NM_198407.2(GHSR):c.847C>T (p.Arg283Ter) rs148371213

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