ClinVar Miner

List of variants in gene SCARB2 reported as benign

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Gene type:
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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_005506.4(SCARB2):c.-174C>T rs1465922 0.55684
NM_005506.4(SCARB2):c.-90G>A rs11547135 0.34117
NM_005506.4(SCARB2):c.705-126G>A rs2289513 0.22725
NM_005506.4(SCARB2):c.705-74A>G rs2289512 0.22710
NM_005506.4(SCARB2):c.613-270C>T rs61598131 0.22693
NM_005506.4(SCARB2):c.824+167A>G rs11947701 0.22689
NM_005506.4(SCARB2):c.613-77A>G rs6532232 0.22676
NM_005506.4(SCARB2):c.423+249G>A rs7677231 0.22675
NM_005506.4(SCARB2):c.994+26T>C rs3821981 0.22639
NM_005506.4(SCARB2):c.994+82G>A rs41284767 0.22633
NM_005506.4(SCARB2):c.825-123C>T rs3733258 0.22631
NM_005506.4(SCARB2):c.825-108G>A rs3733257 0.22629
NM_005506.4(SCARB2):c.1187+245C>G rs60157651 0.21290
NM_005506.4(SCARB2):c.1113+14T>A rs35369082 0.21009
NM_005506.4(SCARB2):c.1114-299G>C rs7679797 0.20410
NM_005506.4(SCARB2):c.118-79C>T rs3733259 0.18056
NM_005506.4(SCARB2):c.118-208C>T rs11729334 0.18016
NM_005506.4(SCARB2):c.118-292C>T rs6835324 0.16517
NM_005506.4(SCARB2):c.424-210A>G rs3816248 0.12932
NM_005506.4(SCARB2):c.704+217T>G rs28563976 0.12639
NM_005506.4(SCARB2):c.994+154T>C rs13119254 0.10657
NM_005506.4(SCARB2):c.612+227T>C rs894247 0.10651
NM_005506.4(SCARB2):c.423+101G>C rs2304814 0.10648
NM_005506.4(SCARB2):c.824+101G>A rs34334700 0.10555
NM_005506.4(SCARB2):c.704+254G>A rs2053487 0.10550
NM_005506.4(SCARB2):c.424-43T>C rs894248 0.10549
NM_005506.4(SCARB2):c.1240-53A>G rs35583533 0.09474
NM_005506.4(SCARB2):c.48G>C (p.Leu16=) rs72857097 0.04875
NM_005506.4(SCARB2):c.1399-280C>T rs72655526 0.04170
NM_005506.4(SCARB2):c.1187+81C>G rs74438684 0.02878
NM_005506.4(SCARB2):c.994+249T>C rs17001559 0.02844
NM_005506.4(SCARB2):c.1187+57G>A rs75217148 0.02530
NM_005506.4(SCARB2):c.1186G>A (p.Val396Ile) rs2228380 0.02529
NM_005506.4(SCARB2):c.275+201C>T rs59815580 0.02528
NM_005506.4(SCARB2):c.118-27G>A rs79180365 0.02525
NM_005506.4(SCARB2):c.*117G>A rs3733255 0.02483
NM_005506.4(SCARB2):c.824+258C>T rs73826385 0.02447
NM_005506.4(SCARB2):c.276-169C>T rs75285019 0.02431
NM_005506.4(SCARB2):c.*67C>G rs3733256 0.02430
NM_005506.4(SCARB2):c.1399-220G>T rs75945181 0.02423
NM_005506.4(SCARB2):c.117+115G>A rs150247097 0.01783
NM_005506.4(SCARB2):c.994+48G>C rs147948083 0.01638
NM_005506.4(SCARB2):c.475A>G (p.Met159Val) rs143655258 0.00858
NM_005506.4(SCARB2):c.362G>A (p.Arg121Gln) rs73826386 0.00619
NM_005506.4(SCARB2):c.1239+14C>T rs143699909 0.00432
NM_005506.4(SCARB2):c.171T>C (p.Pro57=) rs199895330 0.00232
NM_005506.4(SCARB2):c.445G>A (p.Val149Met) rs147159813 0.00217
NM_005506.4(SCARB2):c.704+16T>C rs199686576 0.00148
NM_005506.4(SCARB2):c.246G>C (p.Arg82=) rs35035064 0.00116
NM_005506.4(SCARB2):c.486C>T (p.Ala162=) rs143518519 0.00054
NM_005506.4(SCARB2):c.567T>C (p.His189=) rs141208366 0.00037
NM_005506.4(SCARB2):c.275+7C>T rs777137419 0.00026
NM_005506.4(SCARB2):c.-23C>G rs377635707 0.00014
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.33G>T (p.Thr11=) rs774721226 0.00001
NM_005506.4(SCARB2):c.-27C>G rs553389773
NM_005506.4(SCARB2):c.117+296del rs78406257
NM_005506.4(SCARB2):c.1188-250C>A rs7664889
NM_005506.4(SCARB2):c.1399-169_1399-167del rs3836573
NM_005506.4(SCARB2):c.1399-178T>A rs3755890
NM_005506.4(SCARB2):c.423+135C>T rs2304813
NM_005506.4(SCARB2):c.995-53_995-49del rs57802484

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