ClinVar Miner

List of variants reported as likely benign for Hyperinsulinemic hypoglycemia, familial, 4

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_005327.7(HADH):c.636+13G>A rs17511214 0.04139
NM_005327.4(HADH):c.*818A>G rs17511319 0.03973
NM_005327.4(HADH):c.-193G>A rs10017687 0.02168
NM_005327.4(HADH):c.-65G>A rs28703310 0.01115
NM_005327.7(HADH):c.*600C>T rs544321475 0.00077
NM_005327.7(HADH):c.*514A>G rs183594888 0.00020
NM_005327.7(HADH):c.*383G>C rs550706321 0.00001
NM_005327.7(HADH):c.*660_*661del

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