>gnl|dbSNP|ss24648907|allelePos=101|len=201|taxid=9606|alleles='C/G'|mol=Genomic
AGGGTGATCT TCTGTTCTAG GGAGAAAGTG TCTCATTTGC AGAAAGGAAA GGCACCTGCG
GTATTTGTGA AATGCCATGA CAAGTCTC
TGAATAAGAA GT
S
AGGCTGGTGA GC
ATTCTGGGCT AAAGCTGACT GGGCATCCTG AGCTTGCACC CTAAGGGAGG CAGCTTCATG
CATTCCTCTT CACCCCATCA CCAGCAGC
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 | 44 | 44 | C=0.72727275
| G=0.27272728 | C/C=0.54545456 C/G=0.36363637 G/G=0.09090909
| Pr(chiSq=0.153,df=1) =0.752 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 42 | 42 | C=0.95238096
| G=0.04761905 | C/C=0.90476191 C/G=0.09523810
| Pr(chiSq=0.005,df=1) =1.000 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 46 | 46 | C=0.93478262
| G=0.06521739 | C/C=0.86956519 C/G=0.13043478
| Pr(chiSq=0.014,df=1) =1.000 | Genotype Freq. |