a<p>haplotype defined by AAGGAA at rs4586379, rs2035645, rs4777974, rs11637898, rs11074070, and rs3784735.</p>b<p>haplotype defined by TTAGT at rs4586379, rs8025225, rs11074066, rs11074067, and rs2035645.</p>c<p>haplotype defined by GCAACC at rs4586379, rs2035645, rs4777974, rs11637898, rs11074070, and rs3784735.</p>d<p>haplotype defined by CCCCG at rs4586379, rs8025225, rs11074066, rs11074067, and rs2035645.</p
Motivation: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-...
<p>N/A = Data not provided</p><p><sup>a</sup> Bonferroni corrected <i>P</i> = 0.164</p><p>VO = ‘Von ...
<p>Frequencies of inferred haplotypes among the cases and controls and their association with risk N...
<p>Freq = haplotype frequency, Beta = regression coefficient, Stat = Test statistic (T), p = p-value...
<p>Column: Hap-Score shows haplotype score statistic; Base, part of the baseline; Frequencies and di...
<p>Column: Hap-Score shows haplotype score statistic; Base, part of the baseline; Frequencies and di...
<p>The haplotype frequencies were comparable to those specified in the CEU HapMap dataset. Subjects ...
<p>n = number of haplotypes in the population.</p><p>HR, Hazard Ratio; CI, Confidence Interval.</p
<p>LD blocks are indicated in black triangles, with red shading indicating high LD (D′) for CEU geno...
<p>Column: Hap-Score shows haplotype score statistic; Base, part of the baseline; Frequencies and di...
<p><b>Copyright information:</b></p><p>Taken from "Mutation and evolutionary analyses identify candi...
a<p>The sequence of the SNPs in the Haplotypes was rs2227983, rs2072454, rs17337023, rs1050171, rs11...
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
a<p>The sequence of the SNPs in the Haplotypes was rs2227983, rs2072454, rs17337023, rs1050171, rs11...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
Motivation: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-...
<p>N/A = Data not provided</p><p><sup>a</sup> Bonferroni corrected <i>P</i> = 0.164</p><p>VO = ‘Von ...
<p>Frequencies of inferred haplotypes among the cases and controls and their association with risk N...
<p>Freq = haplotype frequency, Beta = regression coefficient, Stat = Test statistic (T), p = p-value...
<p>Column: Hap-Score shows haplotype score statistic; Base, part of the baseline; Frequencies and di...
<p>Column: Hap-Score shows haplotype score statistic; Base, part of the baseline; Frequencies and di...
<p>The haplotype frequencies were comparable to those specified in the CEU HapMap dataset. Subjects ...
<p>n = number of haplotypes in the population.</p><p>HR, Hazard Ratio; CI, Confidence Interval.</p
<p>LD blocks are indicated in black triangles, with red shading indicating high LD (D′) for CEU geno...
<p>Column: Hap-Score shows haplotype score statistic; Base, part of the baseline; Frequencies and di...
<p><b>Copyright information:</b></p><p>Taken from "Mutation and evolutionary analyses identify candi...
a<p>The sequence of the SNPs in the Haplotypes was rs2227983, rs2072454, rs17337023, rs1050171, rs11...
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
a<p>The sequence of the SNPs in the Haplotypes was rs2227983, rs2072454, rs17337023, rs1050171, rs11...
<p>Allelic components of the presented haplotypes are rs3787138, rs1044396 and rs3787140 SNPs, respe...
Motivation: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-...
<p>N/A = Data not provided</p><p><sup>a</sup> Bonferroni corrected <i>P</i> = 0.164</p><p>VO = ‘Von ...
<p>Frequencies of inferred haplotypes among the cases and controls and their association with risk N...