>gnl|dbSNP|ss24385598|allelePos=101|len=201|taxid=9606|alleles='A/C'|mol=Genomic
ATCTGCCTAC TCTCCTCCAC GTGCAGGCCA AGAGCACTGA AGACACCCTG GTCCTCCCGG
AAGGGCAGTC CCACAGGCAG CGGCACCC
ATTTCTGGGC CC
M
GCCACAGGAC GT
CCGATGGGAG AGCTTGTCTG GCTCTACTGA TGATGGATAG GCCCCTTCCT GAGCCTTGGT
GTCCCTGGAA TGAGGAAAGA TTCTCCAT
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 | A=0.58333331
| C=0.41666666 | A/C=0.41666666 A/A=0.37500000 C/C=0.20833333
| Pr(chiSq=0.490,df=1) =0.527 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | A=0.93478262
| C=0.06521739 | A/A=0.86956519 A/C=0.13043478
| Pr(chiSq=0.014,df=1) =1.000 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.62500000
| A=0.37500000 | C/C=0.41666666 A/C=0.41666666 A/A=0.16666667
| Pr(chiSq=0.296,df=1) =0.655 | Genotype Freq. |