List of variants reported as benign for Leber congenital amaurosis 7 by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_000554.6(CRX):c.*1455T>A	rs10418834	0.68727
NM_000554.6(CRX):c.*2183T>C	rs7259671	0.68119
NM_000554.6(CRX):c.*966G>C	rs3933489	0.35856
NM_000554.6(CRX):c.*2106C>T	rs12982537	0.35558
NM_000554.6(CRX):c.*400A>T	rs3848536	0.32741
NM_000554.6(CRX):c.*1346G>A	rs12462534	0.32243
NM_000554.6(CRX):c.*579T>C	rs4356586	0.32205
NM_000554.6(CRX):c.*401A>C	rs3848537	0.31847
NM_000554.6(CRX):c.*682C>T	rs3859431	0.31819
NM_000554.6(CRX):c.*2559G>C	rs12463238	0.31236
NM_000554.6(CRX):c.*2704C>T	rs12974951	0.31186
NM_000554.6(CRX):c.*2717G>T	rs11666203	0.30498
NM_000554.6(CRX):c.*3017C>T	rs11666244	0.30306
NM_000554.6(CRX):c.*3301T>C	rs11670620	0.30261
NM_000554.6(CRX):c.*3279C>T	rs11666316	0.30253
NM_000554.6(CRX):c.*1122G>C	rs73576710	0.17992
NM_000554.6(CRX):c.*769G>A	rs55835533	0.17955
NM_000554.6(CRX):c.100+12C>T	rs62128766	0.14108
NM_000554.6(CRX):c.*2171C>T	rs77875912	0.12286
NM_000554.6(CRX):c.*2380C>T	rs62128810	0.12202
NM_000554.6(CRX):c.*1046C>T	rs62128808	0.12194
NM_000554.6(CRX):c.*1289G>A	rs62128809	0.12192
NM_000554.6(CRX):c.*3285C>G	rs62128811	0.12171
NM_000554.6(CRX):c.*679G>A	rs112202398	0.12071
NM_000554.6(CRX):c.*3238G>A	rs4081725	0.05457
NM_000554.6(CRX):c.*1792C>T	rs56226622	0.04477
NM_000554.6(CRX):c.101-12A>G	rs73941294	0.01428
NM_000554.6(CRX):c.*2155G>A	rs113560570
NM_000554.6(CRX):c.*2937T>C	rs7248427
NM_000554.6(CRX):c.*591G>C	rs3859430

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