ClinVar Miner

List of variants in gene GHSR reported as uncertain significance 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: 21
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NM_198407.2(GHSR):c.*1046T>A rs756728640
NM_198407.2(GHSR):c.*1268T>C rs755925335
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.*1815C>G rs762604209
NM_198407.2(GHSR):c.*1832G>A rs886058178
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.*758G>A rs886058183
NM_198407.2(GHSR):c.*813A>G rs147683685
NM_198407.2(GHSR):c.*829C>A rs535110477
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.271C>T (p.Leu91Phe) rs79053943
NM_198407.2(GHSR):c.709A>T (p.Arg237Trp) rs199588904
NM_198407.2(GHSR):c.847C>T (p.Arg283Ter) rs148371213

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