List of variants reported as uncertain significance for Porencephaly 2; Hemorrhage, intracerebral, susceptibility to by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001846.4(COL4A2):c.2395C>T (p.Pro799Ser)	rs376694121	0.00004
NM_001846.4(COL4A2):c.360+1G>A	rs759305120	0.00002
NM_001846.4(COL4A2):c.4906G>A (p.Gly1636Ser)	rs753412782	0.00001
NM_001846.4(COL4A2):c.1363G>A (p.Ala455Thr)
NM_001846.4(COL4A2):c.2594C>G (p.Pro865Arg)
NM_001846.4(COL4A2):c.3206G>A (p.Arg1069Gln)

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