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. 2014 Aug 21;24(1):128–141. doi: 10.1093/hmg/ddu424

Table 2.

Statistical analysis of the genotyping results from both C57/Bl6 Crb1rd8/rd8 lines 1 and 2 with either high (n = 11) or low (n = 11) number of autofluorescent fundus lesions

SNP Position in bp/Chr. 15 P-value
rs13459176 3279130 1.01E−04
CEL-15_8331158 8474279 1.03E−04
CEL-15_9687257 9788004 6.22E−04
rs13482431 11311464 6.22E−04
rs3711814 13219494 6.22E−04
CEL-15_15482356 15577251 9.27E−05
rs13482455 16731203 9.27E−05
rs13482469 20942406 9.27E−05
rs13482477 22519205 9.27E−05
rs13482485 25450871 9.27E−05
rs13482504 30322280 2.91E−04
rs13482509 32042169 2.91E−04
rs6188239 34331233 2.91E−04
rs3695416 38484397 2.91E−04
CEL-15_43206205 43188178 2.91E−04
rs13482543 43870893 2.91E−04
rs13482558 47166660 2.91E−04
rs13482571 49998375 2.91E−04

Listed are all informative SNPs that showed significant differences between the two groups based on a Pearson's χ2 test indicating the genomic region on chromosome 15 that is associated with the incidence of the AF-lesions phenotype.