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Table 1 Identified significant rare genetic variants for Q1

From: Pathway-based joint effects analysis of rare genetic variants using Genetic Analysis Workshop 17 exon sequence data

SNP

Chromosome

Position

MAF

P-value

β (standard error)

In causal gene?

C13S524

13

27,899,915

0.0043

2.33 × 10−7

1.92 (0.37)

Yes (FLT1)

C2S2355

2

112,864,155

0.0087

6.43 × 10−7

1.31 (0.26)

No (RGPD8)

C2S2174

2

107,855,174

0.0094

2.66 × 10−6

1.04 (0.22)

No (RGPD4)

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BMC Proceedings

ISSN: 1753-6561

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