ClinVar Miner

List of variants in gene IHH reported as benign for not provided

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_002181.4(IHH):c.578-235G>A rs427587 0.98975
NM_002181.4(IHH):c.1128T>C (p.Thr376=) rs394452 0.85910
NM_002181.4(IHH):c.577+81dup rs34694069 0.58735
NM_002181.4(IHH):c.753T>C (p.Pro251=) rs3731881 0.58582
NM_002181.4(IHH):c.600G>A (p.Thr200=) rs3731878 0.10242
NM_002181.4(IHH):c.577+99G>T rs114758192 0.06047
NM_002181.4(IHH):c.316-226T>C rs59423734 0.03780
NM_002181.4(IHH):c.755A>G (p.His252Arg) rs76479554 0.02052
NM_002181.4(IHH):c.969C>T (p.His323=) rs76578869 0.01963
NM_002181.4(IHH):c.819C>T (p.Pro273=) rs61747697 0.00915
NM_002181.4(IHH):c.315+8C>T rs186249490 0.00278
NM_002181.4(IHH):c.*25G>T rs76709099 0.00219
NM_002181.4(IHH):c.*83A>T rs538403599 0.00219
NM_002181.4(IHH):c.873G>A (p.Arg291=) rs149554120 0.00182
NM_002181.4(IHH):c.1051G>A (p.Val351Met) rs143959492 0.00174
NM_002181.4(IHH):c.618C>T (p.Ala206=) rs3731879 0.00163
NM_002181.4(IHH):c.858G>A (p.Pro286=) rs146055831 0.00083
NM_002181.4(IHH):c.857C>T (p.Pro286Leu) rs140093604 0.00080
NM_002181.4(IHH):c.228G>A (p.Glu76=) rs150747743 0.00048
NM_002181.4(IHH):c.*175C>G rs3099
NM_002181.4(IHH):c.1128= (p.Thr376=)
NM_002181.4(IHH):c.316-153G>T rs72967954

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