List of variants reported as benign for Alport syndrome 1, X-linked recessive by Mendelics

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Total variants: 4

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HGVS	dbSNP
NM_000092.5(COL4A4):c.3979G>A (p.Val1327Met)	rs2229813
NM_033380.3(COL4A5):c.2107A>G (p.Ile703Val)	rs104886155
NM_033380.3(COL4A5):c.2215C>G (p.Pro739Ala)	rs104886164
NM_033380.3(COL4A5):c.2999G>T (p.Gly1000Val)	rs281874709

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