>gnl|dbSNP|ss24556460|allelePos=101|len=201|taxid=9606|alleles='A/C'|mol=Genomic
GCTCTTGAAG CAGCTCAGGG TGAAGCCTCC ACTGACCTAC ACTCAACAGA TGATCTTCAC
ACAATCTCTG AGGGATCTGA CTCTTTGA
GACCTACTGA AG
M
TGCTCCTCAT GA
CAGTTTCTAA GAGGTCAGAG GAGACTGGTG GGCTCAACTC AGGACAGAAA ACCAGAAGCT
CTGAGCTCTG CTCATGTTCC TACCCTCT
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=0.52083331
| A=0.47916666 | A/C=0.45833334 C/C=0.29166666 A/A=0.25000000
| Pr(chiSq=0.160,df=1) =0.752 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | C=0.76086956
| A=0.23913044 | C/C=0.60869563 A/C=0.30434781 A/A=0.08695652
| Pr(chiSq=0.616,df=1) =0.439 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.72916669
| A=0.27083334 | C/C=0.58333331 A/C=0.29166666 A/A=0.12500000
| Pr(chiSq=1.642,df=1) =0.200 | Genotype Freq. |