ClinVar Miner

List of variants in gene OCA2 reported as benign for not specified

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_000275.3(OCA2):c.1183-4A>G rs10852218 0.71746
NM_000275.3(OCA2):c.1065G>A (p.Ala355=) rs1800404 0.59023
NM_000275.3(OCA2):c.1551C>T (p.Cys517=) rs1800411 0.54427
NM_000275.3(OCA2):c.1365-15C>T rs12910433 0.51222
NM_000275.3(OCA2):c.2328T>C (p.Ala776=) rs1800419 0.47440
NM_000275.3(OCA2):c.2364G>A (p.Ser788=) rs12592307 0.19938
NM_000275.3(OCA2):c.913C>T (p.Arg305Trp) rs1800401 0.07659
NM_000275.3(OCA2):c.2058A>C (p.Ala686=) rs1800416 0.05476
NM_000275.3(OCA2):c.1256G>A (p.Arg419Gln) rs1800407 0.04917
NM_000275.3(OCA2):c.2244+18A>G rs41304383 0.03776
NM_000275.3(OCA2):c.1952-16A>G rs113151152 0.01792
NM_000275.3(OCA2):c.2165T>C (p.Ile722Thr) rs1800417 0.01681
NM_000275.3(OCA2):c.1113C>T (p.Gly371=) rs1800405 0.01593
NM_000275.3(OCA2):c.1844A>G (p.His615Arg) rs1800414 0.01432
NM_000275.3(OCA2):c.796C>T (p.Arg266Trp) rs33929465 0.00876
NM_000275.3(OCA2):c.1752C>T (p.His584=) rs151225947 0.00803
NM_000275.3(OCA2):c.79G>A (p.Gly27Arg) rs61738394 0.00532
NM_000275.3(OCA2):c.1857C>T (p.Asp619=) rs7164127 0.00070
NM_000275.3(OCA2):c.2208G>A (p.Ser736=) rs1800418
NM_000275.3(OCA2):c.722C>G (p.Pro241Arg) rs2305253

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