List of variants reported as benign for Autosomal recessive cerebellar ataxia by Illumina Laboratory Services, Illumina

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_020247.4(COQ8A):c.*815C>T	rs10495274	0.53093
NM_020247.5(COQ8A):c.1660-9T>C	rs7552783	0.45219
NM_020247.5(COQ8A):c.1716T>C (p.Ser572=)	rs3738725	0.42035
NM_021830.5(TWNK):c.-605G>T	rs3740484	0.35155
NM_020247.5(COQ8A):c.*464G>A	rs8159	0.31059
NM_021830.5(TWNK):c.*766A>T	rs3740488	0.28823
NM_021830.5(TWNK):c.1593-5C>T	rs3740485	0.28642
NM_021830.5(TWNK):c.1593-3T>C	rs3740486	0.28631
NM_020247.5(COQ8A):c.117G>A (p.Ala39=)	rs11549708	0.16388
NM_021830.5(TWNK):c.*521C>G	rs11542131	0.08029
NM_021830.5(TWNK):c.1102G>A (p.Val368Ile)	rs17113613	0.04615
NM_021830.5(TWNK):c.*204G>A	rs61871507	0.01328
NM_018319.3(TDP1):c.-276_-274dupCCG	rs35210768
NM_018319.4(TDP1):c.*608del	rs397897279
NM_020247.4(COQ8A):c.807_808insT	rs3215920
NM_020247.5(COQ8A):c.*389dup	rs11420839

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