List of variants in gene CSTB reported as likely benign for not provided

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000100.4(CSTB):c.67-324G>A	rs6378	0.01165
NM_000100.4(CSTB):c.168+53C>T	rs180832281	0.01164
NM_000100.4(CSTB):c.*69A>G	rs142767585	0.00798
NM_000100.4(CSTB):c.121G>A (p.Val41Met)	rs143153487	0.00101
NM_000100.4(CSTB):c.*19C>T	rs6384	0.00013
NM_000100.4(CSTB):c.183C>T (p.Asp61=)	rs772899788	0.00009
NM_000100.4(CSTB):c.67-12C>T	rs776841907	0.00004
NC_000021.9:g.43773905del	rs201363469
NC_000021.9:g.43773924_43773925del	rs202136987
NM_000100.4(CSTB):c.67-175dup	rs201742249

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