List of variants reported as pathogenic for hemorrhage, intracerebral, susceptibility to

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000789.4(ACE):c.2371C>T (p.Arg791Ter)	rs397514689	0.00002
NM_000789.4(ACE):c.1473_1475delinsA (p.Asp491fs)	rs1599142041
NM_000789.4(ACE):c.3521del (p.Gly1174fs)	rs754265941
NM_000789.4(ACE):c.444_445insTTAGC (p.Arg149fs)	rs778759606
NM_000789.4(ACE):c.793C>T (p.Arg265Ter)
NM_001845.6(COL4A1):c.2317G>A (p.Gly773Arg)	rs672601347
NM_001845.6(COL4A1):c.2987G>A (p.Gly996Asp)
NM_012330.4(KAT6B):c.5040C>G (p.Tyr1680Ter)	rs369027010

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