List of variants studied for Brain small vessel disease 1 with or without ocular anomalies by Baylor Genetics

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001845.6(COL4A1):c.169C>T (p.Gln57Ter)
NM_001845.6(COL4A1):c.1991-2A>G	rs2139169623
NM_001845.6(COL4A1):c.2086G>A (p.Gly696Ser)	rs587780588
NM_001845.6(COL4A1):c.2458+1G>A	rs1878012979
NM_001845.6(COL4A1):c.2662G>A (p.Gly888Arg)	rs797045034
NM_001845.6(COL4A1):c.2788G>A (p.Gly930Ser)	rs2139163058
NM_001845.6(COL4A1):c.3077G>C (p.Gly1026Ala)	rs1877834496
NM_001845.6(COL4A1):c.3139G>C (p.Gly1047Arg)
NM_001845.6(COL4A1):c.3218G>A (p.Gly1073Asp)	rs1877801384
NM_001845.6(COL4A1):c.3353G>A (p.Gly1118Asp)	rs1566349690
NM_001845.6(COL4A1):c.3358A>G (p.Lys1120Glu)	rs1566349683
NM_001845.6(COL4A1):c.3555A>G (p.Lys1185=)	rs1057518654
NM_001845.6(COL4A1):c.3770G>A (p.Gly1257Glu)	rs1877518903
NM_001845.6(COL4A1):c.4591A>G (p.Met1531Val)	rs1343193102
NM_001845.6(COL4A1):c.460_461delinsAT (p.Gly154Met)
NM_001845.6(COL4A1):c.4887C>G (p.Tyr1629Ter)	rs542803991

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