Table I.

Retrospective genome-wide mapping of known mHag loci by zygosity-genotype correlation analysis

mHag
SNP
Frequency (literature)
Frequency (in 14 trios)
Number of trios
Useful number of individuals
Locus: number of r2 = 1 SNPs
Source
  % %     
HMSD rs9945924 35.6 31 11 30 reference 12  
ACC-1Y rs1138357 46.5* 47.6 10 23 reference 8  
ACC-2 rs3826007 44.5* 47.6 10 23 reference 8  
ADIR rs2296377 37 42.9 13 27 reference 20  
HA-8 rs2173904 70.2* 64.3 10 16 11 reference 21  
HB-1Y rs161557 46.3* 14.3 14 41 reference 22  
mHag
SNP
Frequency (literature)
Frequency (in 14 trios)
Number of trios
Useful number of individuals
Locus: number of r2 = 1 SNPs
Source
  % %     
HMSD rs9945924 35.6 31 11 30 reference 12  
ACC-1Y rs1138357 46.5* 47.6 10 23 reference 8  
ACC-2 rs3826007 44.5* 47.6 10 23 reference 8  
ADIR rs2296377 37 42.9 13 27 reference 20  
HA-8 rs2173904 70.2* 64.3 10 16 11 reference 21  
HB-1Y rs161557 46.3* 14.3 14 41 reference 22  

Results of the correlation analyses for six mHags. Published phenotype frequencies are derived from Spierings et al. (19; *) or from the indicated reference. Analyses were performed as described in Fig. 4. Depicted is the minimal number of trios (Number of trios) resulting in only a single genome locus with 100% correlation, together with the number of CEPH individuals for whom zygosity data was available (Useful number of individuals). Also depicted is the number of SNPs with 100% correlation that was found at this genome locus (Locus: number of r2 = 1 SNPs).

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