>gnl|dbSNP|ss23186100|allelePos=101|len=201|taxid=9606|alleles='G/C'|mol=Genomic
GTAACTTGCT GATATGTGAA GCGTGCTTCA GTTCATACCT ATTCAAAAGA GGACAGTCTC
AGAAGAGGCC TTCACACTGG GCTCTCGA
AACCAACAGT TT
S
ATTAGGAGAA TA
AGATCAGATA CAGAGATGAG ATAAAAGTCC ACAAAACCCA GACCATCTAA ACTGCTCAGG
CTCCCTCCTG AGTTTCTGGA ACTGTTCC
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=0.64583331
| G=0.35416666 | C/G=0.45833334 C/C=0.41666666 G/G=0.12500000
| Pr(chiSq=0.000,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | C=0.52173913
| G=0.47826087 | C/C=0.39130434 G/G=0.34782609 C/G=0.26086956
| Pr(chiSq=5.239,df=1) =0.025 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | G=0.85416669
| C=0.14583333 | G/G=0.70833331 C/G=0.29166666
| Pr(chiSq=0.189,df=1) =0.752 | Genotype Freq. |