>gnl|dbSNP|ss23145067|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
AGAGAGCTCA AGGGCTCGCT CCACAGGGAA GGCTGGAGTG GGGGATGACT AATGCAATTA
CCCATTTGGA ATTTAGCTTA GAAGATGA
AAAGAAATAG AC
Y
AGAGGTGACA GG
CTTAAAAATT CCTTTTTTTT TTTTTTTTGG TTTGTTCCCA ATCCTCTCCT AGTCCAGTGT
TGGGAGAGGA GCTGCGGTAA GGAGAGTG
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=0.75000000
| T=0.25000000 | C/C=0.62500000 C/T=0.25000000 T/T=0.12500000
| Pr(chiSq=2.667,df=1) =0.150 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | C=0.63043481
| T=0.36956522 | C/C=0.47826087 C/T=0.30434781 T/T=0.21739130
| Pr(chiSq=2.767,df=1) =0.100 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | T=0.64583331
| C=0.35416666 | T/T=0.50000000 C/T=0.29166666 C/C=0.20833333
| Pr(chiSq=3.153,df=1) =0.100 | Genotype Freq. |