ClinVar Miner

List of variants in gene DAG1 reported as likely benign for Limb-girdle muscular dystrophy-dystroglycanopathy, type C9; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 9

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Total variants: 29
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HGVS dbSNP
NM_004393.6(DAG1):c.1026C>T (p.Pro342=) rs1553652858
NM_004393.6(DAG1):c.1212G>A (p.Thr404=) rs139781017
NM_004393.6(DAG1):c.1287A>G (p.Val429=) rs200282503
NM_004393.6(DAG1):c.1308G>A (p.Thr436=) rs143763229
NM_004393.6(DAG1):c.1641C>T (p.Gly547=) rs374490206
NM_004393.6(DAG1):c.1752C>A (p.Gly584=) rs769750924
NM_004393.6(DAG1):c.1773C>T (p.Phe591=) rs2229010
NM_004393.6(DAG1):c.1785C>T (p.Val595=) rs762148188
NM_004393.6(DAG1):c.183T>C (p.Val61=) rs775928044
NM_004393.6(DAG1):c.1905C>T (p.Phe635=) rs577609846
NM_004393.6(DAG1):c.2036G>A (p.Arg679His) rs113904914
NM_004393.6(DAG1):c.2082C>T (p.Asn694=) rs146453412
NM_004393.6(DAG1):c.2313C>T (p.Ala771=) rs764289801
NM_004393.6(DAG1):c.2322C>T (p.Cys774=) rs759442412
NM_004393.6(DAG1):c.2415C>T (p.Asp805=) rs749427996
NM_004393.6(DAG1):c.243C>G (p.Thr81=) rs202047972
NM_004393.6(DAG1):c.2451C>G (p.Leu817=) rs886042761
NM_004393.6(DAG1):c.24G>A (p.Ser8=) rs1229832209
NM_004393.6(DAG1):c.2511C>T (p.Pro837=) rs778665335
NM_004393.6(DAG1):c.258G>C (p.Leu86Phe) rs145403829
NM_004393.6(DAG1):c.278T>C (p.Ile93Thr) rs149218670
NM_004393.6(DAG1):c.286-10del rs747305463
NM_004393.6(DAG1):c.294G>A (p.Ala98=) rs752506833
NM_004393.6(DAG1):c.402C>T (p.Ser134=) rs367603470
NM_004393.6(DAG1):c.510C>A (p.Ala170=) rs147153370
NM_004393.6(DAG1):c.57C>T (p.Leu19=) rs768105958
NM_004393.6(DAG1):c.591C>T (p.Ala197=) rs768487898
NM_004393.6(DAG1):c.599C>G (p.Thr200Ser) rs41290704
NM_004393.6(DAG1):c.636C>T (p.His212=) rs765923041

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