>gnl|dbSNP|ss24090954|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
TGGAGGCTGC TCAATGACCC AGAAGACCTC TAACCCCTTC TGAATATAGA AGAATGAGTA
TAGATACCCT CTGAAGACAC ATTTCACT
TCTGCATAAC TT
Y
AATTCTATGT CT
TGATCTTTTG TATCTTAAAT CTCTATTCCC TTCAGAATTA TCAGATTTTC TATTTCCTCT
GCCCTTTGAT GACCTCCTTG AGCCTCCG
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 | T=0.77083331
| C=0.22916667 | T/T=0.58333331 C/T=0.37500000 C/C=0.04166667
| Pr(chiSq=0.091,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | T=0.86956519
| C=0.13043478 | T/T=0.78260869 C/T=0.17391305 C/C=0.04347826
| Pr(chiSq=1.252,df=1) =0.273 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.52083331
| T=0.47916666 | C/T=0.37500000 C/C=0.33333334 T/T=0.29166666
| Pr(chiSq=1.484,df=1) =0.251 | Genotype Freq. |