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

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Total variants: 6

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HGVS	dbSNP
NM_033380.3(COL4A5):c.1855C>T (p.Pro619Ser)	rs1569494314
NM_033380.3(COL4A5):c.2858G>T (p.Gly953Val)	rs78972735
NM_033380.3(COL4A5):c.4200A>G (p.Gly1400=)	rs1603318167
NM_033380.3(COL4A5):c.4300C>A (p.Leu1434Met)	rs1569508163
NM_033380.3(COL4A5):c.891+9T>G	rs779787322
NM_138715.3(MSR1):c.877C>T (p.Arg293Ter)	rs41341748

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