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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 28

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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.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.5726G>C (p.Ser1909Thr)	rs74685771	0.00700
NM_198576.4(AGRN):c.5598C>T (p.Thr1866=)	rs17778478	0.00691
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.1123G>T (p.Ala375Ser)	rs138031468	0.00517
NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu)	rs144620006	0.00426
NM_198576.4(AGRN):c.773C>T (p.Thr258Ile)	rs200607541	0.00231
NM_198576.4(AGRN):c.3285C>G (p.Thr1095=)	rs149957221	0.00179
NM_198576.4(AGRN):c.2805+7G>A	rs190000918	0.00177
NM_198576.4(AGRN):c.4116C>T (p.Ala1372=)	rs200170414	0.00170
NM_198576.4(AGRN):c.5832C>T (p.Thr1944=)	rs143373928	0.00131
NM_198576.4(AGRN):c.2266G>A (p.Ala756Thr)	rs140764403	0.00079
NM_198576.4(AGRN):c.2796C>T (p.Asn932=)	rs147153797	0.00031
NM_198576.4(AGRN):c.4731G>A (p.Pro1577=)	rs115885544	0.00006
NM_198576.4(AGRN):c.3264G>C (p.Leu1088Phe)	rs150132566

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