>gnl|dbSNP|ss24243900|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
TGAGGCGGCA CTAGTGGGCA GGACGGAGCC AAAGGATTTT CCACAGGAAC TCAAATGCTT
AAGGGCCCCA AGGTATCAAT ATTTAAGG
AGTGCCTGCC TT
Y
CACGCATAGT GG
TCTAGGGAGA CAAGCCTATG CTATGGGCCA TGCTGGAGCT TCTTTGCTCA AAAGTGACAT
AACTTTTTTT TTTTTTTTTT TTGGGAAA
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=0.66666669
| T=0.33333334 | C/T=0.50000000 C/C=0.41666666 T/T=0.08333334
| Pr(chiSq=0.375,df=1) =0.584 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | T=0.76086956
| C=0.23913044 | T/T=0.52173913 C/T=0.47826087
| Pr(chiSq=0.957,df=1) =0.343 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | T=0.75000000
| C=0.25000000 | T/T=0.54166669 C/T=0.41666666 C/C=0.04166667
| Pr(chiSq=0.296,df=1) =0.655 | Genotype Freq. |