List of variants in gene AGRN reported by Athena Diagnostics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_198576.4(AGRN):c.5358T>C (p.Gly1786=)	rs17160781	0.07808
NM_198576.4(AGRN):c.804C>T (p.Ala268=)	rs113789806	0.04323
NM_198576.4(AGRN):c.5070C>T (p.Phe1690=)	rs17160776	0.04120
NM_198576.4(AGRN):c.2183A>T (p.Glu728Val)	rs113288277	0.02922
NM_198576.4(AGRN):c.4977-10A>G	rs142286944	0.01820
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.729C>G (p.Gly243=)	rs191270495	0.00928
NM_198576.4(AGRN):c.1528G>A (p.Gly510Ser)	rs138288952	0.00834
NM_198576.4(AGRN):c.5598C>T (p.Thr1866=)	rs17778478	0.00691
NM_198576.4(AGRN):c.67G>C (p.Val23Leu)	rs201073369	0.00674
NM_198576.4(AGRN):c.3465T>C (p.Ala1155=)	rs146358566	0.00648
NM_198576.4(AGRN):c.3866C>T (p.Pro1289Leu)	rs139294803	0.00637
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	0.00406
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.2067G>A (p.Gln689=)	rs139886237	0.00282
NM_198576.4(AGRN):c.1434G>A (p.Thr478=)	rs147346337	0.00281
NM_198576.4(AGRN):c.4131C>T (p.Phe1377=)	rs368555478	0.00225
NM_198576.4(AGRN):c.2690C>T (p.Ala897Val)	rs116836855	0.00200
NM_198576.4(AGRN):c.1570C>T (p.Arg524Trp)	rs144164397	0.00119
NM_198576.4(AGRN):c.3765G>A (p.Ala1255=)	rs149490453	0.00107
NM_198576.4(AGRN):c.2277G>A (p.Pro759=)	rs199985558	0.00032
NM_198576.4(AGRN):c.4138C>T (p.Arg1380Cys)	rs747790893	0.00007
NM_198576.4(AGRN):c.1534G>A (p.Ala512Thr)	rs780205618	0.00002
NM_198576.4(AGRN):c.3264G>C (p.Leu1088Phe)	rs150132566

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