ClinVar Miner

List of variants in gene APOL1 studied for Focal segmental glomerulosclerosis 4, susceptibility to

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_003661.4(APOL1):c.573C>T (p.Leu191=) rs150846072 0.00220
NM_003661.4(APOL1):c.318T>C (p.Asn106=) rs141898256 0.00069
NM_003661.4(APOL1):c.1116G>A (p.Lys372=) rs201657348 0.00066
NM_003661.4(APOL1):c.1182G>A (p.Ala394=) rs185040686 0.00061
NM_003661.4(APOL1):c.797T>G (p.Leu266Arg) rs142955744 0.00036
NM_003661.4(APOL1):c.1150A>T (p.Ile384Phe) rs373463596 0.00019
NM_003661.4(APOL1):c.967G>C (p.Glu323Gln) rs200395416 0.00008
NM_003661.4(APOL1):c.1051T>C (p.Tyr351His) rs375837468 0.00006
NM_003661.4(APOL1):c.315-7T>C rs190240132 0.00006
NM_003661.4(APOL1):c.390C>T (p.His130=) rs760970273 0.00005
NM_003661.4(APOL1):c.837T>C (p.Ile279=) rs371302335 0.00004
NM_003661.4(APOL1):c.1104T>G (p.Ala368=) rs1428826948 0.00001
NM_003661.4(APOL1):c.334C>T (p.Arg112Cys) rs146078613 0.00001
NM_003661.3(APOL1):c.[1024A>G;1152T>G]
NM_003661.4(APOL1):c.1048G>A (p.Val350Ile) rs2146313032
NM_003661.4(APOL1):c.1164_1169del (p.Asn388_Tyr389del) rs71785313
NM_003661.4(APOL1):c.1181C>G (p.Ala394Gly) rs138178894
NM_003661.4(APOL1):c.188-14T>A rs136163
NM_003661.4(APOL1):c.188-14T>G rs136163
NM_003661.4(APOL1):c.314+14G>T rs370874898
NM_003661.4(APOL1):c.945T>G (p.Gly315=) rs1603482264
NM_003661.4(APOL1):c.976A>G (p.Ile326Val) rs1569534160

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