List of variants in gene SCARB2 reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_005506.3(SCARB2):c.-321A>C	rs557285209	0.01605
NM_005506.4(SCARB2):c.994+280A>G	rs144228170	0.01260
NM_005506.4(SCARB2):c.117+74T>A	rs145736175	0.00767
NM_005506.4(SCARB2):c.-148G>C	rs28681268	0.00704
NM_005506.4(SCARB2):c.1187+95T>G	rs192412983	0.00687
NM_005506.4(SCARB2):c.276-272C>T	rs116170711	0.00657
NC_000004.12:g.76213890C>T	rs577208630	0.00570
NM_005506.4(SCARB2):c.705-183G>T	rs17001566	0.00443
NM_005506.4(SCARB2):c.1239+14C>T	rs143699909	0.00432
NM_005506.4(SCARB2):c.1399-206A>G	rs60271776	0.00344
NM_005506.4(SCARB2):c.1188-259C>G	rs111562116	0.00311
NM_005506.4(SCARB2):c.995-79G>A	rs76059298	0.00270
NM_005506.4(SCARB2):c.445G>A (p.Val149Met)	rs147159813	0.00217
NM_005506.4(SCARB2):c.-11C>T	rs200947751	0.00068
NM_005506.4(SCARB2):c.424-4G>A	rs368869126	0.00060
NM_005506.4(SCARB2):c.276-7C>G	rs200507087	0.00042
NM_005506.4(SCARB2):c.567T>C (p.His189=)	rs141208366	0.00037
NM_005506.4(SCARB2):c.424-5C>T	rs192876326	0.00014
NM_005506.4(SCARB2):c.430A>T (p.Ile144Leu)	rs117600063	0.00012
NM_005506.4(SCARB2):c.1187+18C>T	rs202159028	0.00009
NM_005506.4(SCARB2):c.1385G>A (p.Gly462Glu)	rs117157204	0.00009
NM_005506.4(SCARB2):c.275+20T>C	rs377180838	0.00009
NM_005506.4(SCARB2):c.402A>G (p.Arg134=)	rs778684185	0.00009
NM_005506.4(SCARB2):c.915G>A (p.Thr305=)	rs762138695	0.00004
NM_005506.4(SCARB2):c.9A>G (p.Arg3=)	rs148558907	0.00004
NM_005506.4(SCARB2):c.1240-20C>T	rs1372161374	0.00001
NC_000004.12:g.76213847A>G	rs573424919
NM_005506.4(SCARB2):c.-58C>A	rs185028681
NM_005506.4(SCARB2):c.1188-11del	rs796052945
NM_005506.4(SCARB2):c.1399-10T>G	rs1578711063
NM_005506.4(SCARB2):c.553T>C (p.Leu185=)	rs1578723137

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