ClinVar Miner

List of variants in gene SCARB2 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 51
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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.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.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.80G>A (p.Arg27Gln) rs368906199 0.00009
NM_005506.4(SCARB2):c.1187+12T>C rs532651260 0.00006
NM_005506.4(SCARB2):c.-18C>T rs543249957 0.00004
NM_005506.4(SCARB2):c.-44C>A rs1477651224 0.00004
NM_005506.4(SCARB2):c.1089T>C (p.His363=) rs753197792 0.00004
NM_005506.4(SCARB2):c.1240-18A>G rs371940249 0.00004
NM_005506.4(SCARB2):c.1273C>T (p.Leu425=) rs764452245 0.00004
NM_005506.4(SCARB2):c.915G>A (p.Thr305=) rs762138695 0.00004
NM_005506.4(SCARB2):c.93G>A (p.Lys31=) rs558215488 0.00004
NM_005506.4(SCARB2):c.9A>G (p.Arg3=) rs148558907 0.00004
NM_005506.4(SCARB2):c.468C>T (p.Ile156=) rs771468161 0.00003
NM_005506.4(SCARB2):c.275+14A>G rs759250571 0.00002
NM_005506.4(SCARB2):c.291A>G (p.Lys97=) rs377635556 0.00002
NM_005506.4(SCARB2):c.824+20G>A rs1257697437 0.00002
NM_005506.4(SCARB2):c.904T>C (p.Leu302=) rs377511764 0.00002
NM_005506.4(SCARB2):c.117+14G>A rs772998739 0.00001
NM_005506.4(SCARB2):c.1194G>A (p.Thr398=) rs574498998 0.00001
NM_005506.4(SCARB2):c.1240-20C>T rs1372161374 0.00001
NM_005506.4(SCARB2):c.423+7A>C rs1380805649 0.00001
NM_005506.4(SCARB2):c.704+17A>G rs762520392 0.00001
NM_005506.4(SCARB2):c.705-20C>G rs747460425 0.00001
NC_000004.12:g.76213847A>G rs573424919
NM_005506.4(SCARB2):c.-48G>A rs1057522858
NM_005506.4(SCARB2):c.-58C>A rs185028681
NM_005506.4(SCARB2):c.1188-11del rs796052945
NM_005506.4(SCARB2):c.1398+10_1398+22del rs778683141
NM_005506.4(SCARB2):c.228C>G (p.Leu76=) rs35069772
NM_005506.4(SCARB2):c.897A>G (p.Ala299=) rs1057520962
NM_005506.4(SCARB2):c.927C>T (p.Ala309=) rs775395230
NM_005506.4(SCARB2):c.9A>T (p.Arg3=) rs148558907

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