ClinVar Miner

Variants in gene AGRN with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 45
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HGVS dbSNP gnomAD frequency
NM_198576.4(AGRN):c.5358T>C (p.Gly1786=) rs17160781 0.08292
NM_198576.4(AGRN):c.3516+10G>C rs76264143 0.05034
NM_198576.4(AGRN):c.4996G>A (p.Val1666Ile) rs17160775 0.04750
NM_198576.4(AGRN):c.1058A>G (p.Gln353Arg) rs150359724 0.01713
NM_198576.4(AGRN):c.4740C>T (p.Arg1580=) rs115019873 0.01570
NM_198576.4(AGRN):c.3570C>T (p.Arg1190=) rs75361935 0.01197
NM_198576.4(AGRN):c.2025C>G (p.Gly675=) rs28484890 0.01118
NM_198576.4(AGRN):c.2406C>T (p.Gly802=) rs75774767 0.01095
NM_198576.4(AGRN):c.4452C>T (p.Thr1484=) rs75767981 0.01049
NM_198576.4(AGRN):c.1528G>A (p.Gly510Ser) rs138288952 0.00834
NM_198576.4(AGRN):c.4695G>C (p.Gln1565His) rs199876002 0.00827
NM_198576.4(AGRN):c.738C>T (p.Asp246=) rs536085218 0.00811
NM_198576.4(AGRN):c.5223C>T (p.Gly1741=) rs147681220 0.00805
NM_198576.4(AGRN):c.3964C>T (p.Arg1322Trp) rs184970403 0.00799
NM_198576.4(AGRN):c.3972G>A (p.Pro1324=) rs201483077 0.00799
NM_198576.4(AGRN):c.4540G>A (p.Ala1514Thr) rs111818381 0.00781
NM_198576.4(AGRN):c.1660G>A (p.Val554Met) rs79016973 0.00706
NM_198576.4(AGRN):c.5726G>C (p.Ser1909Thr) rs74685771 0.00700
NM_198576.4(AGRN):c.1603+19G>A rs115191992 0.00697
NM_198576.4(AGRN):c.5598C>T (p.Thr1866=) rs17778478 0.00691
NM_198576.4(AGRN):c.3077C>A (p.Thr1026Asn) rs3813188 0.00690
NM_198576.4(AGRN):c.3465T>C (p.Ala1155=) rs146358566 0.00657
NM_198576.4(AGRN):c.3866C>T (p.Pro1289Leu) rs139294803 0.00637
NM_198576.4(AGRN):c.3404A>G (p.Gln1135Arg) rs142416636 0.00588
NM_198576.4(AGRN):c.67G>C (p.Val23Leu) rs201073369 0.00583
NM_198576.4(AGRN):c.5352C>T (p.Phe1784=) rs112073270 0.00537
NM_198576.4(AGRN):c.5025C>T (p.Gly1675=) rs147990356 0.00536
NM_198576.4(AGRN):c.1123G>T (p.Ala375Ser) rs138031468 0.00517
NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu) rs144620006 0.00426
NM_198576.4(AGRN):c.4285C>T (p.Arg1429Cys) rs201346452 0.00327
NM_198576.4(AGRN):c.4839C>T (p.Cys1613=) rs113020870 0.00302
NM_198576.4(AGRN):c.1993G>A (p.Glu665Lys) rs143324306 0.00297
NM_198576.4(AGRN):c.2067G>A (p.Gln689=) rs139886237 0.00288
NM_198576.4(AGRN):c.1434G>A (p.Thr478=) rs147346337 0.00281
NM_198576.4(AGRN):c.800C>T (p.Thr267Met) rs566673314 0.00265
NM_198576.4(AGRN):c.773C>T (p.Thr258Ile) rs200607541 0.00231
NM_198576.4(AGRN):c.4131C>T (p.Phe1377=) rs368555478 0.00225
NM_198576.4(AGRN):c.2690C>T (p.Ala897Val) rs116836855 0.00203
NM_198576.4(AGRN):c.3765G>A (p.Ala1255=) rs149490453 0.00113
NM_198576.4(AGRN):c.1188G>A (p.Pro396=) rs138841641 0.00103
NM_198576.4(AGRN):c.2266G>A (p.Ala756Thr) rs140764403 0.00079
NM_198576.4(AGRN):c.4323G>A (p.Ala1441=) rs373287346 0.00066
NM_198576.4(AGRN):c.4298+11A>T rs369279324 0.00005
NM_198576.4(AGRN):c.2457G>C (p.Gly819=) rs112039851
NM_198576.4(AGRN):c.3264G>C (p.Leu1088Phe) rs150132566

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