List of variants in gene combination LOC126860782, SETX reported as benign for autosomal recessive disease

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_015046.7(SETX):c.7200-10dup	rs531485265
NM_015046.7(SETX):c.7200-11_7200-10del	rs531485265
NM_015046.7(SETX):c.7203C>T (p.Phe2401=)
NM_015046.7(SETX):c.7204C>G (p.Leu2402Val)	rs1402767850
NM_015046.7(SETX):c.7222T>C (p.Leu2408=)

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