>gnl|dbSNP|ss23896282|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
CAAATAGTGA CCACTAAAAG TCACAAAGAG AAAACAAAAA TATATGATTT TATGATTTAC
AAGTAATATA GAACATAAAA CATTTATT
TTATCTATTT AC
Y
TATTGCCTAC AT
TTCCTATGTA ACTATTGCCT ATATTTGACG ATTGTTGAAC TACAAAAACA GCAATTTCAG
ATGGTTCAAC CCAGTATTTA TTTGTTTA
Population ID -Class | Total Sample (2N) | Founder (2N) | Major Allele Freq. | Minor Allele Freq. | Genotype Freq. | HWE Goodness of Fit | Data Source | AFD_EUR_PANEL - NORTH AMERICA | 48 | 48 | C=0.95833331
| T=0.04166667 | C/C=0.91666669 C/T=0.08333334
| Pr(chiSq=0.004,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 44 | 44 | C=0.77272725
| T=0.22727273 | C/C=0.63636363 C/T=0.27272728 T/T=0.09090909
| Pr(chiSq=1.099,df=1) =0.317 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.75000000
| T=0.25000000 | C/C=0.50000000 C/T=0.50000000
| Pr(chiSq=1.167,df=1) =0.294 | Genotype Freq. |