ClinVar Miner

List of variants in gene AGRN reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_198576.3(AGRN):c.*19C>T rs3121561
NM_198576.3(AGRN):c.1058A>G (p.Gln353Arg) rs150359724
NM_198576.3(AGRN):c.1178-6T>C rs2799066
NM_198576.3(AGRN):c.1385-15_1385-14delCT rs35881187
NM_198576.3(AGRN):c.1528G>A (p.Gly510Ser) rs138288952
NM_198576.3(AGRN):c.202-13A>G rs115704555
NM_198576.3(AGRN):c.2183A>T (p.Glu728Val) rs113288277
NM_198576.3(AGRN):c.2254+16G>A rs114389542
NM_198576.3(AGRN):c.2457G>C (p.Gly819=) rs112039851
NM_198576.3(AGRN):c.2555A>G (p.Gln852Arg) rs9697293
NM_198576.3(AGRN):c.261C>T (p.Asp87=) rs6657048
NM_198576.3(AGRN):c.3066A>G (p.Ser1022=) rs2465128
NM_198576.3(AGRN):c.3264G>C (p.Leu1088Phe) rs150132566
NM_198576.3(AGRN):c.3516+10G>C rs76264143
NM_198576.3(AGRN):c.3517-12T>C rs3128102
NM_198576.3(AGRN):c.3558T>C (p.Phe1186=) rs10267
NM_198576.3(AGRN):c.3964C>T (p.Arg1322Trp) rs184970403
NM_198576.3(AGRN):c.3972G>A (p.Pro1324=) rs201483077
NM_198576.3(AGRN):c.4161T>C (p.Thr1387=) rs9442391
NM_198576.3(AGRN):c.4298+17C>T rs188005130
NM_198576.3(AGRN):c.4514+16G>C rs112917612
NM_198576.3(AGRN):c.4540G>A (p.Ala1514Thr) rs111818381
NM_198576.3(AGRN):c.45G>T (p.Pro15=) rs115173026
NM_198576.3(AGRN):c.4740C>T (p.Arg1580=) rs115019873
NM_198576.3(AGRN):c.4745-17C>T rs2275813
NM_198576.3(AGRN):c.4977-10A>G rs142286944
NM_198576.3(AGRN):c.4996G>A (p.Val1666Ile) rs17160775
NM_198576.3(AGRN):c.5025C>T (p.Gly1675=) rs147990356
NM_198576.3(AGRN):c.5070C>T (p.Phe1690=) rs17160776
NM_198576.3(AGRN):c.5353G>A (p.Asp1785Asn) rs144245019
NM_198576.3(AGRN):c.5358T>C (p.Gly1786=) rs17160781
NM_198576.3(AGRN):c.5598C>T (p.Thr1866=) rs17778478
NM_198576.3(AGRN):c.5651+5C>T rs9803031
NM_198576.3(AGRN):c.6057C>T (p.Asp2019=) rs4275402
NM_198576.3(AGRN):c.729C>G (p.Gly243=) rs191270495
NM_198576.3(AGRN):c.804C>T (p.Ala268=) rs113789806

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