List of variants reported as benign for cone-rod dystrophy 11 by Illumina Laboratory Services, Illumina

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_001319074.4(RAX2):c.*866C>T	rs917545	0.78969
NM_001319074.4(RAX2):c.*1366C>G	rs6510769	0.25783
NM_001319074.4(RAX2):c.*785G>A	rs917546	0.20551
NM_001319074.4(RAX2):c.*720G>A	rs917547	0.16734
NM_001319074.4(RAX2):c.*1149C>T	rs1860322	0.15969
NM_001319074.4(RAX2):c.217-8C>T	rs79588413	0.15214
NM_001319074.4(RAX2):c.*680G>A	rs28673245	0.06699
NM_001319074.4(RAX2):c.*902G>T	rs10405125	0.02418
NM_001319074.4(RAX2):c.155C>T (p.Pro52Leu)	rs76076446	0.01485
NM_001319074.4(RAX2):c.*647T>C	rs112369501	0.01352
NM_001319074.4(RAX2):c.*381A>G	rs73531473	0.01319
NM_001319074.4(RAX2):c.45T>G (p.Gly15=)	rs139127905	0.00435
NM_001319074.4(RAX2):c.*1324A>G	rs138882802	0.00293
NM_001319074.4(RAX2):c.-270C>T	rs776666200	0.00265
NM_001319074.4(RAX2):c.*689C>T	rs115071988	0.00201
NM_001319074.4(RAX2):c.*45C>T	rs139146360	0.00120
NM_001319074.4(RAX2):c.282C>T (p.Ala94=)	rs201021639	0.00102
NM_001319074.4(RAX2):c.*191C>T	rs150808899	0.00099
NM_001319074.4(RAX2):c.156G>A (p.Pro52=)	rs141804618	0.00059
NM_001319074.4(RAX2):c.-281G>A	rs182965071	0.00048
NM_001319074.4(RAX2):c.-316G>A	rs576680324	0.00048
NM_001319074.4(RAX2):c.*1169G>A	rs554924169	0.00031
NM_001319074.4(RAX2):c.*1054C>T	rs368356816	0.00005
NM_001319074.4(RAX2):c.*679C>T	rs576669713	0.00001
NM_001319074.4(RAX2):c.217-10C>T	rs772762463	0.00001

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