>gnl|dbSNP|ss23145060|allelePos=101|len=201|taxid=9606|alleles='G/C'|mol=Genomic
CCTTGTCACA TTTGTCTGGT TTTGTTTTTC TATAGAAAAT CAAAGCAAAC AAAGCAGCTC
TCAGTAATGC ATTCTAAAAC TGTCATGA
ATTAACTGAC CT
S
TGTAGAAATT TC
CTTTTCCTGG GTCAATTCAG CAATTTTGTC CTGCTTGTTG TTTTCTAAAT ACATCAGTTT
CATTTTGTGT TGAACATCAA AGCCCTCA
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 | C=0.79166669
| G=0.20833333 | C/C=0.62500000 C/G=0.33333334 G/G=0.04166667
| Pr(chiSq=0.003,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 44 | 44 | C=0.77272725
| G=0.22727273 | C/C=0.54545456 C/G=0.45454547
| Pr(chiSq=0.767,df=1) =0.403 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.81250000
| G=0.18750000 | C/C=0.70833331 C/G=0.20833333 G/G=0.08333334
| Pr(chiSq=2.400,df=1) =0.150 | Genotype Freq. |