ClinVar Miner

List of variants in gene MEFV reported as likely benign for not provided

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Gene type:
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Total variants: 25
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HGVS dbSNP
NM_000243.2(MEFV):c.*9C>T rs11466048
NM_000243.2(MEFV):c.-13C>G rs200991336
NM_000243.2(MEFV):c.-330G>A rs11466013
NM_000243.2(MEFV):c.1092G>A (p.Pro364=) rs11466022
NM_000243.2(MEFV):c.1092G>T (p.Pro364=) rs11466022
NM_000243.2(MEFV):c.1223G>A (p.Arg408Gln) rs11466024
NM_000243.2(MEFV):c.1467G>A (p.Gln489=) rs61732424
NM_000243.2(MEFV):c.1518C>T (p.Ile506=) rs104895099
NM_000243.2(MEFV):c.1587+18C>T rs11466030
NM_000243.2(MEFV):c.1587+33C>G rs146820856
NM_000243.2(MEFV):c.1611-134G>C
NM_000243.2(MEFV):c.1727-16C>G
NM_000243.2(MEFV):c.1760-8C>T rs1567231839
NM_000243.2(MEFV):c.1770G>A (p.Leu590=)
NM_000243.2(MEFV):c.1827C>G (p.Pro609=) rs104895135
NM_000243.2(MEFV):c.2163C>T (p.Phe721=) rs11466047
NM_000243.2(MEFV):c.329T>C (p.Leu110Pro) rs11466018
NM_000243.2(MEFV):c.333G>A (p.Gly111=) rs61732425
NM_000243.2(MEFV):c.414A>T (p.Gly138=)
NM_000243.2(MEFV):c.42G>A (p.Glu14=) rs113314808
NM_000243.2(MEFV):c.442G>C (p.Glu148Gln) rs3743930
NM_000243.2(MEFV):c.549G>A (p.Pro183=) rs587781035
NM_000243.2(MEFV):c.564C>T (p.Pro188=) rs775755423
NM_000243.2(MEFV):c.786T>C (p.Thr262=) rs575521131
NM_000243.2(MEFV):c.911-12G>A rs372016564

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