ClinVar Miner

List of variants in gene combination GHR, LOC107963950 reported as uncertain significance for Laron syndrome

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_000163.5(GHR):c.-176A>G rs1314535276 0.00004
NM_000163.5(GHR):c.-118C>T rs1050201240
NM_000163.5(GHR):c.-74C>T rs892049573
NM_000163.5(GHR):c.-76C>T rs1742723526
NM_000163.5(GHR):c.-89G>T rs1033209852

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