ClinVar Miner

List of variants in gene AGRN reported as likely benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_198576.4(AGRN):c.1058A>G (p.Gln353Arg) rs150359724
NM_198576.4(AGRN):c.1123G>T (p.Ala375Ser) rs138031468
NM_198576.4(AGRN):c.2025C>G (p.Gly675=) rs28484890
NM_198576.4(AGRN):c.2406C>T (p.Gly802=) rs75774767
NM_198576.4(AGRN):c.261C>T (p.Asp87=) rs6657048
NM_198576.4(AGRN):c.2805+7G>A rs190000918
NM_198576.4(AGRN):c.3264G>C (p.Leu1088Phe) rs150132566
NM_198576.4(AGRN):c.3285C>G (p.Thr1095=) rs149957221
NM_198576.4(AGRN):c.3404A>G (p.Gln1135Arg) rs142416636
NM_198576.4(AGRN):c.3465T>C (p.Ala1155=) rs146358566
NM_198576.4(AGRN):c.3516+10G>C rs76264143
NM_198576.4(AGRN):c.3570C>T (p.Arg1190=) rs75361935
NM_198576.4(AGRN):c.3866C>T (p.Pro1289Leu) rs139294803
NM_198576.4(AGRN):c.3964C>T (p.Arg1322Trp) rs184970403
NM_198576.4(AGRN):c.3972G>A (p.Pro1324=) rs201483077
NM_198576.4(AGRN):c.4116C>T (p.Ala1372=) rs200170414
NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu) rs144620006
NM_198576.4(AGRN):c.4452C>T (p.Thr1484=) rs75767981
NM_198576.4(AGRN):c.4540G>A (p.Ala1514Thr) rs111818381
NM_198576.4(AGRN):c.4731G>A (p.Pro1577=) rs115885544
NM_198576.4(AGRN):c.4740C>T (p.Arg1580=) rs115019873
NM_198576.4(AGRN):c.4996G>A (p.Val1666Ile) rs17160775
NM_198576.4(AGRN):c.5358T>C (p.Gly1786=) rs17160781
NM_198576.4(AGRN):c.5598C>T (p.Thr1866=) rs17778478
NM_198576.4(AGRN):c.5726G>C (p.Ser1909Thr) rs74685771
NM_198576.4(AGRN):c.5832C>T (p.Thr1944=) rs143373928
NM_198576.4(AGRN):c.773C>T (p.Thr258Ile) rs200607541

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