List of variants in gene combination LOC130009366, SACS reported as likely benign for not provided

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_014363.6(SACS):c.171+6C>T	rs3751368	0.13186
NM_014363.6(SACS):c.171+24G>A	rs182487544	0.00964
NM_014363.6(SACS):c.21-41G>T	rs569423976	0.00430
NM_014363.6(SACS):c.171+13C>T	rs374672041	0.00347
NM_014363.6(SACS):c.99T>C (p.Asp33=)	rs775206528	0.00016
NM_014363.6(SACS):c.141G>A (p.Ser47=)	rs1593160882	0.00001
NM_014363.6(SACS):c.21-162C>G	rs578105700

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