List of variants reported as benign for Leber congenital amaurosis by Illumina Clinical Services Laboratory,Illumina

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Total variants: 40

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HGVS	dbSNP
NM_000554.5(CRX):c.-116T>C	rs10418215
NM_000554.6(CRX):c.*1122G>C	rs73576710
NM_000554.6(CRX):c.*1346G>A	rs12462534
NM_000554.6(CRX):c.*1455T>A	rs10418834
NM_000554.6(CRX):c.*1900del	rs796977583
NM_000554.6(CRX):c.*2106C>T	rs12982537
NM_000554.6(CRX):c.*2171C>T	rs77875912
NM_000554.6(CRX):c.*2183T>C	rs7259671
NM_000554.6(CRX):c.*2559G>C	rs12463238
NM_000554.6(CRX):c.*2704C>T	rs12974951
NM_000554.6(CRX):c.*2717G>T	rs11666203
NM_000554.6(CRX):c.*2937T>C	rs7248427
NM_000554.6(CRX):c.*3017C>T	rs11666244
NM_000554.6(CRX):c.308_310AAG[2]	rs398059782
NM_000554.6(CRX):c.*3238G>A	rs4081725
NM_000554.6(CRX):c.*3279C>T	rs11666316
NM_000554.6(CRX):c.*3301T>C	rs11670620
NM_000554.6(CRX):c.*400A>T	rs3848536
NM_000554.6(CRX):c.*401A>C	rs3848537
NM_000554.6(CRX):c.*579T>C	rs4356586
NM_000554.6(CRX):c.*591G>C	rs3859430
NM_000554.6(CRX):c.*682C>T	rs3859431
NM_000554.6(CRX):c.*769G>A	rs55835533
NM_000554.6(CRX):c.*966G>C	rs3933489
NM_000554.6(CRX):c.100+12C>T	rs62128766
NM_001122769.3(LCA5):c.-62A>G	rs2803195
NM_001122769.3(LCA5):c.71T>C (p.Leu24Ser)	rs2655655
NM_003322.6(TULP1):c.*318T>G	rs1051952
NM_003322.6(TULP1):c.200C>G (p.Thr67Arg)	rs7764472
NM_003322.6(TULP1):c.783G>C (p.Lys261Asn)	rs2064318
NM_020366.3(RPGRIP1):c.3097G>C (p.Glu1033Gln)	rs3748361
NM_020366.3(RPGRIP1):c.574A>G (p.Lys192Glu)	rs6571751
NM_025114.3(CEP290):c.2512A>G (p.Lys838Glu)	rs11104738
NM_025114.3(CEP290):c.3574-9delT	rs10717563
NM_025114.3(CEP290):c.6522+12dupT	rs11405846
NM_025114.3(CEP290):c.853-12_853-11insG	rs71082425
NM_183059.2(RD3):c.-204_-203insC	rs11463656
NM_201253.3(CRB1):c.*28T>C	rs41302107
NM_201253.3(CRB1):c.2128+15A>C	rs75691013
NM_201253.3(CRB1):c.71-12A>T	rs12042179

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