>gnl|dbSNP|ss23842239|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
TTCATATGTG ATCCCTATGG TGTTGTCCTA CAATCACCTA ATTCAGAATC ACTAGGTGTG
TTTGTTTAAA ATGGAGATTT CTGGTCTC
TGTACCAGGC AT
Y
GTGATTCAGG AC
TTATGTGTAT CACAACCAGG CATATATATT TTCAACAAGT TTCCCATGTG ATTCTAATGC
ATATGAGAGT TTCGGAACCA TAGGTCTA
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 | C=0.54347825
| T=0.45652175 | C/T=0.39130434 C/C=0.34782609 T/T=0.26086956
| Pr(chiSq=1.028,df=1) =0.317 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | T=0.60869563
| C=0.39130434 | C/T=0.43478259 T/T=0.39130434 C/C=0.17391305
| Pr(chiSq=0.175,df=1) =0.752 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 46 | 46 | C=0.52173913
| T=0.47826087 | C/T=0.43478259 C/C=0.30434781 T/T=0.26086956
| Pr(chiSq=0.381,df=1) =0.584 | Genotype Freq. |