List of variants in gene SCARB2 reported as benign for epilepsy

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_005506.4(SCARB2):c.1113+14T>A	rs35369082	0.21009
NM_005506.4(SCARB2):c.424-43T>C	rs894248	0.10549
NM_005506.4(SCARB2):c.48G>C (p.Leu16=)	rs72857097	0.04875
NM_005506.4(SCARB2):c.1186G>A (p.Val396Ile)	rs2228380	0.02529
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.704+16T>C	rs199686576	0.00148
NM_005506.4(SCARB2):c.246G>C (p.Arg82=)	rs35035064	0.00116
NM_005506.4(SCARB2):c.275+7C>T	rs777137419	0.00026
NM_005506.4(SCARB2):c.275+20T>C	rs377180838	0.00009

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