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

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_005506.4(SCARB2):c.445G>A (p.Val149Met)	rs147159813	0.00217
NM_005506.4(SCARB2):c.246G>C (p.Arg82=)	rs35035064	0.00116
NM_005506.4(SCARB2):c.382C>G (p.Pro128Ala)	rs143558324	0.00114
NM_005506.4(SCARB2):c.1187+18C>T	rs202159028	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.93G>A (p.Lys31=)	rs558215488	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.33G>T (p.Thr11=)	rs774721226	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
NM_005506.4(SCARB2):c.-48G>A	rs1057522858
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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