>gnl|dbSNP|ss23326605|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
GTGACACTTT GTGTGTTGGG TGGAGGCTGG TTCGCCAGAA GGCTTTTTCT TAATATCCAT
TCTCAGCTTT AGGTCTTTAT TTTACACT
ATGCCTTAGA GA
Y
GGTCTCTTTC CA
TACTCATTTA ATTCTTCCAC CATTACTAAC TGTTACTTGT TACTTAATGC TTGTTAGAGT
GGTGGCGTGG GGTCAGGAGT CCATTCTT
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=0.81250000
| T=0.18750000 | C/C=0.66666669 C/T=0.29166666 T/T=0.04166667
| Pr(chiSq=0.044,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 44 | 44 | C=0.79545456
| T=0.20454545 | C/C=0.68181819 C/T=0.22727273 T/T=0.09090909
| Pr(chiSq=2.001,df=1) =0.200 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.83333331
| T=0.16666667 | C/C=0.70833331 C/T=0.25000000 T/T=0.04166667
| Pr(chiSq=0.240,df=1) =0.655 | Genotype Freq. |