ClinVar Miner

List of variants reported as benign for Laron syndrome by Illumina Laboratory Services, Illumina

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_000163.5(GHR):c.-164A>G rs2940928 0.81907
NM_000163.5(GHR):c.*542_*543insA rs11369980 0.74904
NM_000163.5(GHR):c.*1554G>A rs7442754 0.71972
NM_000163.5(GHR):c.558A>G (p.Gly186=) rs6179 0.64137
NM_000163.5(GHR):c.*300G>A rs2910875 0.43476
NM_000163.5(GHR):c.1630A>C (p.Ile544Leu) rs6180 0.42616
NM_000163.5(GHR):c.*1934T>C rs62372049 0.04177
NM_000163.5(GHR):c.*1770G>C rs144561552 0.03922
NM_000163.5(GHR):c.*1790G>A rs2973016 0.02583
NM_000163.5(GHR):c.*692C>A rs17839373 0.02559
NM_000163.5(GHR):c.1473C>T (p.Ser491=) rs6176 0.02017
NM_000163.5(GHR):c.1319G>T (p.Cys440Phe) rs6182 0.01122
NM_000163.5(GHR):c.1735C>A (p.Pro579Thr) rs6184 0.01120
NM_000163.5(GHR):c.*781T>A rs17839374 0.01117
NM_000163.5(GHR):c.785-9G>A rs34190075 0.01100
NM_000163.5(GHR):c.1098A>G (p.Leu366=) rs116466139 0.00992
NM_000163.5(GHR):c.-39G>C rs527709793 0.00851
NM_000163.5(GHR):c.*693G>A rs113937917 0.00831
NM_000163.5(GHR):c.*2294A>G rs368826175 0.00001
NM_000163.5(GHR):c.*1498TTG[6] rs398064766
NM_000163.5(GHR):c.484G>A (p.Val162Ile) rs6413484

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