List of variants reported as likely benign for Microvascular complications of diabetes, susceptibility to, 3; Hemorrhage, intracerebral, susceptibility to; Renal tubular dysgenesis of genetic origin by Fulgent Genetics, Fulgent Genetics

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Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_000789.4(ACE):c.3387T>C (p.Phe1129=)	rs4362	0.51177
NM_000789.4(ACE):c.1119-8C>T	rs114861086	0.00991
NM_000789.4(ACE):c.1060G>A (p.Gly354Arg)	rs56394458	0.00732
NM_000789.4(ACE):c.2382G>A (p.Ala794=)	rs61738817	0.00669
NM_000789.4(ACE):c.231G>A (p.Ala77=)	rs184457276	0.00629
NM_000789.4(ACE):c.1038G>C (p.Ser346=)	rs34680431	0.00493
NM_000789.4(ACE):c.2979C>T (p.Ile993=)	rs75067113	0.00452
NM_000789.4(ACE):c.1681C>T (p.Arg561Trp)	rs4314	0.00316
NM_000789.4(ACE):c.3801C>T (p.Ile1267=)	rs144242912	0.00150
NM_000789.4(ACE):c.945+16A>G	rs201274031	0.00142
NM_000789.4(ACE):c.3489C>T (p.Ala1163=)	rs4979	0.00130
NM_000789.4(ACE):c.3363T>C (p.Ser1121=)	rs200201337	0.00037
NM_000789.4(ACE):c.177G>A (p.Gln59=)	rs147912715	0.00034
NM_000789.4(ACE):c.3691+10C>T	rs556274739	0.00030
NM_000789.4(ACE):c.1317G>T (p.Leu439=)	rs140529617	0.00020
NM_000789.4(ACE):c.3321T>G (p.Thr1107=)	rs144974035	0.00013
NM_000789.4(ACE):c.3381-4C>T	rs201962955	0.00011
NM_000789.4(ACE):c.477C>T (p.Pro159=)	rs201285321	0.00011
NM_000789.4(ACE):c.1020C>T (p.Pro340=)	rs3730026	0.00009
NM_000789.4(ACE):c.249+16C>G	rs1568035049	0.00003
NM_000789.4(ACE):c.249+15C>G	rs1392845930	0.00002
NM_000789.4(ACE):c.2518C>A (p.Arg840=)	rs3730036

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