>gnl|dbSNP|ss24183126|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
GCACCCACAG GAATAGCTAA AGGGCCCAGC GGTAAGGTTC AGGGGCTTCA TAAGCACACT
CAAACCCAAG CCTGTGTCAT CATCACAT
AACCCTCAAT GA
Y
AGGACTTCAG CT
ATCCAAGGCC ATGTGCTGTG AGCTGGCCTT GGTGTTATCT CCCCACTAAA TTGCAAGCTT
TGAGGCTAGG GATGATGCTG TAAACTTC
Population ID -Class | Total Sample (2N) | Founder (2N) | Major Allele Freq. | Minor Allele Freq. | Genotype Freq. | HWE Goodness of Fit | Data Source | AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.75000000
| T=0.25000000 | C/C=0.54166669 C/T=0.41666666 T/T=0.04166667
| Pr(chiSq=0.296,df=1) =0.655 | Genotype Freq. |
HapMap-CEU | 226 | 226 | C=0.98230088
| T=0.01769911 | C/C=0.96460176 C/T=0.03539823
| Pr(chiSq=0.001,df=1) =1.000 | Genotype Freq. |
HapMap-HCB - EAST ASIA | 86 | 86 | C=0.80232561
| T=0.19767442 | C/C=0.62790698 C/T=0.34883720 T/T=0.02325581
| Pr(chiSq=0.428,df=1) =0.527 | Genotype Freq. |
HapMap-JPT | 172 | 172 | C=0.72674417
| T=0.27325583 | C/C=0.52325583 C/T=0.40697673 T/T=0.06976745
| Pr(chiSq=0.052,df=1) =1.000 | Genotype Freq. |
HAPMAP-CHB | 82 | 82 | C=0.86585367
| T=0.13414635 | C/C=0.73170733 C/T=0.26829270
| Pr(chiSq=0.246,df=1) =0.655 | Genotype Freq. |
HAPMAP-CHD | 170 | 170 | C=0.80000001
| T=0.20000000 | C/C=0.68235296 C/T=0.23529412 T/T=0.08235294
| Pr(chiSq=5.956,df=1) =0.020 | Genotype Freq. |
HAPMAP-GIH | 176 | 176 | C=0.97159094
| T=0.02840909 | C/C=0.94318181 C/T=0.05681818
| Pr(chiSq=0.004,df=1) =1.000 | Genotype Freq. |
HAPMAP-MEX | 100 | 100 | C=0.86000001
| T=0.14000000 | C/C=0.74000001 C/T=0.23999999 T/T=0.02000000
| Pr(chiSq=0.001,df=1) =1.000 | Genotype Freq. |
HAPMAP-MKK | 286 | 286 | C=0.99650347
| T=0.00349650 | C/C=0.99300700 C/T=0.00699301
| Pr(chiSq=0.000,df=1) =1.000 | Genotype Freq. |
HAPMAP-TSI | 176 | 176 | C=0.98863637
| T=0.01136364 | C/C=0.97727275 C/T=0.02272727
| Pr(chiSq=0.000,df=1) =1.000 | Genotype Freq. |