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

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001355436.2(SPTB):c.4618A>C (p.Arg1540=)	rs61989884	0.00322
NM_001355436.2(SPTB):c.2881G>A (p.Val961Ile)	rs149316006	0.00140
NM_001355436.2(SPTB):c.3015C>T (p.Ala1005=)	rs147235045	0.00102
NM_001355436.2(SPTB):c.2060G>A (p.Arg687His)	rs3742602	0.00101
NM_001355436.2(SPTB):c.2937C>T (p.Ser979=)	rs141762497	0.00033
NM_001355436.2(SPTB):c.5943C>T (p.Arg1981=)	rs75000411	0.00013
NM_001355436.2(SPTB):c.4143C>T (p.Ser1381=)	rs148504156	0.00008
NM_001355436.2(SPTB):c.2781G>A (p.Gln927=)	rs368620488	0.00003
NM_001355436.2(SPTB):c.6132G>A (p.Val2044=)	rs747360003	0.00001
NM_001355436.2(SPTB):c.360C>T (p.Leu120=)	rs886038377
NM_001355436.2(SPTB):c.474+13G>A	rs201559808

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