List of variants reported as uncertain significance for cone-rod dystrophy by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_033100.4(CDHR1):c.783G>A (p.Pro261=)	rs147346345	0.00446
NM_000350.3(ABCA4):c.4685T>C (p.Ile1562Thr)	rs1762111	0.00132
NM_000350.3(ABCA4):c.1749G>C (p.Lys583Asn)	rs145265791	0.00005
NM_033100.4(CDHR1):c.862+4A>C	rs1352559639	0.00001
GRCh38/hg38 19q13.32-13.33(chr19:47257435-47886413)x1
GRCh38/hg38 19q13.33(chr19:47794370-47886413)x1
GRCh38/hg38 19q13.33(chr19:47834312-47840923)x1
GRCh38/hg38 Xp11.23(chrX:49222435-49226325)x0
NM_177965.4(CFAP418):c.3G>A (p.Met1Ile)	rs1249678588

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