ClinVar Miner

List of variants reported as likely benign for Vitreoretinopathy

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_004385.5(VCAN):c.1523T>A (p.Ile508Asn) rs143368552 0.00271
NM_004385.5(VCAN):c.*835G>A rs184855903 0.00035
NM_004385.5(VCAN):c.7893A>T (p.Leu2631Phe) rs148063549 0.00019
NM_004385.5(VCAN):c.8634A>G (p.Pro2878=) rs200031614 0.00011
NM_004385.5(VCAN):c.7493G>T (p.Ser2498Ile) rs761405097 0.00010
NM_004385.5(VCAN):c.249C>A (p.Val83=) rs751640388 0.00005
NM_004385.5(VCAN):c.9049G>C (p.Ala3017Pro) rs774896703 0.00005
NM_004385.5(VCAN):c.9481C>G (p.Leu3161Val) rs765359111 0.00005
NM_004385.5(VCAN):c.109T>G (p.Ser37Ala) rs142740596 0.00004
NM_004385.5(VCAN):c.9880+11C>A rs373723999 0.00004
NM_004385.5(VCAN):c.1127A>C (p.Asp376Ala) rs181669993 0.00001
NM_004385.5(VCAN):c.3204C>T (p.Gly1068=) rs142805131 0.00001
NM_004385.5(VCAN):c.3683C>T (p.Ala1228Val) rs200685807 0.00001
NM_004385.5(VCAN):c.4248C>T (p.Leu1416=) rs758617685 0.00001
NM_004385.5(VCAN):c.6269A>G (p.Gln2090Arg) rs767918859 0.00001
NM_004385.5(VCAN):c.7895C>T (p.Thr2632Ile) rs767660495 0.00001
NM_004385.5(VCAN):c.8454G>A (p.Ala2818=) rs773474075 0.00001
NM_004385.5(VCAN):c.*232_*235del rs372079782
NM_004385.5(VCAN):c.6672T>C (p.Asp2224=) rs183187115

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