List of variants in gene AGRN reported by Neuberg Centre For Genomic Medicine, NCGM

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_198576.4(AGRN):c.5410G>A (p.Val1804Met)	rs754158999	0.00003
NM_198576.4(AGRN):c.5645C>T (p.Thr1882Ile)	rs540580770	0.00003
NM_198576.4(AGRN):c.2509G>A (p.Val837Ile)	rs752913194	0.00002
NM_198576.4(AGRN):c.1555G>T (p.Ala519Ser)
NM_198576.4(AGRN):c.1862C>T (p.Pro621Leu)	rs1303230782
NM_198576.4(AGRN):c.2627A>T (p.Lys876Met)
NM_198576.4(AGRN):c.3004G>C (p.Gly1002Arg)	rs757677789
NM_198576.4(AGRN):c.5132C>A (p.Ala1711Glu)	rs749228236

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