Skip to main content
. Author manuscript; available in PMC: 2015 Feb 19.
Published in final edited form as: Hum Genet. 2014 Oct 4;133(12):1513–1523. doi: 10.1007/s00439-014-1490-9

Table 3.

Summary of associated SNPs from genome-wide analyses (47,599 SNPs) excluding 15q.21-22.3

Chr Gene/Nearby Genes1 SNP rs# Position (bp) MA MAF Case/Control OR 95% CI
P-Value
Lower Upper
11 MYO7A rs356418391 76885901 A 0.12/0.04 4.71 2.38 9.32 8.34x10−6
4 INPP4B rs2636675 143224472 G 0.18/0.13 3.23 1.89 5.54 1.97x10−5
4 ASSP8||LOC100130396 rs10016143 149615561 A 0.45/0.38 2.37 1.56 3.59 5.00x10−5
11 MYO7A rs1110331832 76910600 T 0.12/0.06 3.79 1.98 7.28 6.20x10−5
13 LOC101928697 rs77809485 19761359 G 0.11/0.05 3.96 2.02 7.78 6.55x10−5
11 MYO7A rs788716772 76901819 A 0.12/0.06 3.55 1.89 6.69 8.66x10−5

BP-base pair (GRCH37.p13/hg19); MA-minor allele; MAF-minor allele frequency; OR-odds ratio; CI-confidence interval

1

Nearby genes, noted with//, are the closest genes to the associated SNP regardless of distance

2

rs35641839 missense mutation, rs111033183 missense mutation, rs78871677 synonymous mutation