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. 2016 Jul 4;44(3):1963–1971. doi: 10.1111/ejn.13300

Table 2.

Linkage analysis results

Phenotype chr LOD n exp Best SNP Location
L peak width 10 2.814 0.034 rs10509410 Intronic in PAPSS2
R peak width 16 2.339 0.146 rs11861062 Intergenic
M peak width 2 1.118 0.208 rs9288662 Intronic in SP140
L peak amplitude 19 1.912 0.373 rs1293703 3′in DPRX
M peak amplitude 19 2.031 0.390 rs269940 Intronic in NLRP7
R peak width 8 1.996 0.414 rs7015861 Intronic in FAM91A1
M peak amplitude 18 1.827 0.661 rs9945030 Intronic in RP11‐47G4.2
L peak amplitude 16 1.631 0.738 rs226042 Intronic in CRYM
R peak width 13 1.775 0.804 rs7333894 Intergenic
M peak frequency 1 1.980 0.902 rs11161750 Intronic in COL24A1
M peak width 7 0.849 0.941 rs10486813 Intronic in SUGCT
L peak width 18 1.802 0.949 rs676603 Intronic in AQP4‐AS1

Suggestive and significant linkages for the nine phenotypes, along with their chromosomal location (chr), significance based on 1001 permutations (n exp), name of best‐linked SNP and its location relative to genes. PAPSS2, 3′‐phosphoadenosine 5′‐phosphosulfate synthase 2; SP140, SP140 nuclear body protein; DPRX, divergent‐paired related homeobox; NLRP7, NLR family, pyrin domain‐containing 7; FAM91A1, family with sequence similarity 91 member A1; RP11‐47G4.2, gene RP11‐47G4.2; CRYM, crystallin mu; COL24A1, collagen, type XXIV, alpha 1; SUGCT, succinyl‐CoA,glutarate‐CoA transferase; AQP4‐AS1, AQP4 antisense RNA 1. L, left; M, middle; R, right parieto‐occipital region.