>gnl|dbSNP|ss24153794|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
AAACATTAAC TCTACATCCA CTCAGCCAAC AAAGTCAGAA TACAGAGCTC ACATTTTCTG
CTCATACACC AAGGTGTGTT GTATAGTT
AGACCTTTAG TC
Y
CCTAAACAAC CA
AGCAGACAGG CAAACCATTT TCTCCCAATT AATTGACAGA GGTCAATGAC ATTATACAAC
AGGTATGGTT GAAACATTTA TTTTCCAG
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 | 46 | 46 | T=0.84782606
| C=0.15217391 | T/T=0.78260869 C/T=0.13043478 C/C=0.08695652
| Pr(chiSq=5.624,df=1) =0.020 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | T=0.56521738
| C=0.43478259 | T/T=0.39130434 C/T=0.34782609 C/C=0.26086956
| Pr(chiSq=1.965,df=1) =0.200 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | T=0.54166669
| C=0.45833334 | C/T=0.66666669 T/T=0.20833333 C/C=0.12500000
| Pr(chiSq=2.818,df=1) =0.100 | Genotype Freq. |