Variation detected in the DBA/TEC patient cohort within the resequenced region on chromosome 19.

avariant identifier.
bMost frequent (Major) and alternative (minor) allele within our patient cohort.
cas compared to the human reference genome (hg18, build 36.1).
dnumber of heterozygous and homozygous cases, respectively, within our patient cohort.
eallele frequency and sample size (number of analyzed chromosomes), excluding patient samples with undetermined genotype (NN).
fdatabase identifier (dbSNP128) for previously described SNP (http://www.ncbi.nlm.nih.gov/SNP/) or number of novel SNP with subsequently assigned database identifier (dbSNP129) in brackets, respectively.