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. Author manuscript; available in PMC: 2016 Nov 2.
Published in final edited form as: J Neuroimmunol. 2015 Dec 31;291:70–72. doi: 10.1016/j.jneuroim.2015.12.014

Table 1.

CH25H coding variants identified in MS and NMO patients. Genomic coordinates are given from NCBI Build 37.1; dbSNP IDs are provided from build 138 when available; minor allele frequencies (MAF) were obtained from The Exome Aggregation Consortium (ExAC) database. NR, not reported.

Chromosome: Position Nucleotide change Protein change dbSNP ID ExAC MAF
10:90,966,999 C/G p.Q17H – 0.00003
10:90,966,996 C/G p.L18L rs10887932 0.26
10:90,966,828 G/A p.H74H rs45579235 0.003
10:90,966,546 C/T p.A168A rs4078488 0.21
10:90,966,393 G/A p.N219N rs17382301 0.12