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. 2015 Feb 10;10(2):e0118043. doi: 10.1371/journal.pone.0118043

Table 8. MQLS-corrected allele frequencies and case-control association p-values for the top sequencing variants in the sequencing dataset.

Marker Chr Position Case Control Overall p value Gene Function
MAF MAF MAF
rs41291476 10 102762544 0.0104 0.0019 0.0013 1.25E-06 LZTS2 synonymous
rs147224053 15 91503598 0.0104 0.0019 0.0013 1.25E-06 RCCD1 synonymous
rs4548 3 128525253 0.0987 0.0259 0.0525 3.31E-06 RAB7A synonymous
rs11380 12 6601475 0.0156 0.0078 0.0072 4.68E-06 MRPL51 missense
rs201285308 5 176008380 0.0156 0.0078 0.0072 5.00E-06 CDHR2 missense
rs41279402 20 3785672 0.0414 0.0036 0.0108 9.28E-06 CDC25B UTR-3
6_137234733 6 137234733 0.0403 0.0171 0.0199 1.01E-05 PEX7 UTR-3
rs11676272 2 25141538 0.5938 0.4151 0.4619 1.28E-05 ADCY3 missense
rs144407106 6 136710582 0.0511 0.0203 0.0277 1.53E-05 MAP7 synonymous
rs149872991 15 91496233 0.0278 0.005 0.0085 3.74E-05 UNC45A missense
rs147643564 4 175158508 0.0651 0.0195 0.0318 4.67E-05 FBXO8 UTR-3
rs146399677 20 3785297 0.041 0.0076 0.0129 4.89E-05 CDC25B synonymous
rs56400929 10 105762909 0.0104 0 0.001 7.00E-05 SLK missense
rs150358287 20 3687141 0.0894 0.0374 0.0455 7.94E-05 SIGLEC1 stop-gained
rs34270879 10 90673047 0 0.0434 0.0352 9.17E-05 STAMBPL1 missense

Chr = chromosome. MAF = minor allele frequency. Nucleotide position is based upon the UCSC hg19 human reference genome. Gene and Function annotated by SeattleSeq134.