ClinVar Miner

List of variants in gene MARVELD2 reported as likely benign for not specified

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_001038603.3(MARVELD2):c.898T>A (p.Leu300Met) rs72773422 0.00170
NM_001038603.3(MARVELD2):c.1407C>T (p.Tyr469=) rs61736168 0.00127
NM_001038603.3(MARVELD2):c.615C>T (p.Ala205=) rs146796266 0.00126
NM_001038603.3(MARVELD2):c.389T>A (p.Leu130His) rs144717803 0.00114
NM_001038603.3(MARVELD2):c.900G>A (p.Leu300=) rs138680809 0.00096
NM_001038603.3(MARVELD2):c.30G>A (p.Arg10=) rs143592561 0.00023
NM_001038603.3(MARVELD2):c.211A>G (p.Ile71Val) rs150773481 0.00018
NM_001038603.3(MARVELD2):c.592G>A (p.Val198Met) rs201914751 0.00007
NM_001038603.3(MARVELD2):c.306G>A (p.Pro102=) rs181575833 0.00006
NM_001038603.3(MARVELD2):c.60C>T (p.Asp20=) rs1264640823 0.00006
NM_001038603.3(MARVELD2):c.331G>A (p.Asp111Asn) rs397516553 0.00002
NM_001038603.3(MARVELD2):c.494A>G (p.His165Arg) rs727503157 0.00002
NM_001038603.3(MARVELD2):c.1059A>G (p.Ile353Met) rs727503158 0.00001
NM_001038603.3(MARVELD2):c.1095A>G (p.Leu365=) rs727503159 0.00001
NM_001038603.3(MARVELD2):c.1479G>A (p.Leu493=) rs752765358 0.00001
NM_001038603.3(MARVELD2):c.771C>T (p.Leu257=) rs571015098 0.00001
NM_001038603.3(MARVELD2):c.1446G>A (p.Lys482=) rs1554047591
NM_001038603.3(MARVELD2):c.156A>G (p.Pro52=) rs138816138
NM_001038603.3(MARVELD2):c.156A>T (p.Pro52=) rs138816138

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