>gnl|dbSNP|ss24524222|allelePos=101|len=201|taxid=9606|alleles='A/G'|mol=Genomic
TGGTCTGGGC CGCTTCTTCA GCTCTGAGAC CACCGCAGCC CACTCCCTAG GTAAGGGGGA
CCTGTCTGTG CCCCAGCAGC CCCCAGCG
GTCCTGGTGA CC
R
TGCAGGGAGA CG
CAAACATTCT CCCCACGTGT GTTTGGTCAG TTAGTGCAGG AAGATGCCTT TTTTAAGCCC
CAGGGTTTTC TCATCTGTTC AGAATAGT
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 | A=0.60869563
| G=0.39130434 | A/G=0.52173913 A/A=0.34782609 G/G=0.13043478
| Pr(chiSq=0.209,df=1) =0.655 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 44 | 44 | A=0.68181819
| G=0.31818181 | A/A=0.50000000 A/G=0.36363637 G/G=0.13636364
| Pr(chiSq=0.577,df=1) =0.479 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 46 | 46 | A=0.71739131
| G=0.28260869 | A/G=0.47826087 A/A=0.47826087 G/G=0.04347826
| Pr(chiSq=0.741,df=1) =0.403 | Genotype Freq. |