Table 5. .

Validation of the Most Significantly Associated SNPs in a Previously Genotyped Independent Cohort

Base Pair Location	SNP	Gene Location	Qualitative SPH P Value	Quantitative SPH P Value
69425930	rs3803036	Coding nonsyn. in PTPRR	0.73	0.15
71970854	rs1520562	>600 kb from nearest gene	0.075	0.024
76672201	rs1358228	76 kb upstream of NAV3	0.17	0.32
78976016	rs7315130	>100 kb from nearest gene	0.86	0.97
80351222	rs17306116	Intronic PPFIA2	0.82	0.99

The most significantly associated SNPs from our data not included in this table were not present in the independent data set. Base pairs are based on human genome build 36.2, chromosome 12. Methods of this testing and cohort information have been previously published.²⁹