List of variants in gene combination BSCL2, HNRNPUL2-BSCL2 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: 22

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HGVS	dbSNP	gnomAD frequency
NM_001122955.4(BSCL2):c.1137A>G (p.Glu379=)	rs6856	0.16571
NM_001122955.4(BSCL2):c.1280T>C (p.Leu427Pro)	rs145649423	0.00301
NM_001122955.4(BSCL2):c.124C>T (p.Arg42Cys)	rs201493373	0.00061
NM_001122955.4(BSCL2):c.1100C>T (p.Pro367Leu)	rs144245125	0.00048
NM_001122955.4(BSCL2):c.861C>T (p.Leu287=)	rs370926100	0.00016
NM_001122955.4(BSCL2):c.1234+7G>A	rs200631909	0.00011
NM_001122955.4(BSCL2):c.588C>T (p.Cys196=)	rs369806785	0.00011
NM_001122955.4(BSCL2):c.939C>T (p.Ile313=)	rs200300686	0.00010
NM_001122955.4(BSCL2):c.88-19C>T	rs760935362	0.00008
NM_001122955.4(BSCL2):c.1017A>G (p.Arg339=)	rs147902831	0.00004
NM_001122955.4(BSCL2):c.621T>C (p.Ser207=)	rs777598096	0.00004
NM_001122955.4(BSCL2):c.870G>C (p.Leu290=)	rs767104988	0.00004
NM_001122955.4(BSCL2):c.130G>C (p.Gly44Arg)	rs900971126	0.00003
NM_001122955.4(BSCL2):c.88-588T>C	rs970321804	0.00003
NM_001122955.4(BSCL2):c.404+15C>G	rs200598473	0.00002
NM_001122955.4(BSCL2):c.1234+19C>T	rs748453195	0.00001
NM_001122955.4(BSCL2):c.166G>A (p.Gly56Arg)	rs1226106958	0.00001
NM_001122955.4(BSCL2):c.660C>T (p.Leu220=)	rs950978890	0.00001
NM_001122955.4(BSCL2):c.1006-8C>T	rs1057521013
NM_001122955.4(BSCL2):c.306C>T (p.Ile102=)	rs1554985612
NM_001122955.4(BSCL2):c.486+8T>G	rs1238731769
NM_001122955.4(BSCL2):c.810C>T (p.Arg270=)	rs998498207

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