>gnl|dbSNP|ss23803630|allelePos=101|len=201|taxid=9606|alleles='A/G'|mol=Genomic
ACCCAGCTAC GGAGAGGATG AGGCCGGAGC TAATGAAGAA CGTGCCCAGG AAGAGGGAGG
CGGCCACGCG CGGAGCCCCT GCAAACAG
ACACCGCTGA GC
R
GACGGGCAGG AC
GGTGGCCCTG GCTCCTCGCC TGGCCCCCGG TGCCCCCTGC ACATGGCAGA TGCGCTGCTC
TCTGAACATG CCTGAGCCTC ACGGGACC
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 | G=0.79166669
| A=0.20833333 | G/G=0.62500000 A/G=0.33333334 A/A=0.04166667
| Pr(chiSq=0.003,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 40 | 40 | G=0.62500000
| A=0.37500000 | G/G=0.50000000 A/G=0.25000000 A/A=0.25000000
| Pr(chiSq=4.356,df=1) =0.050 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | G=0.81250000
| A=0.18750000 | G/G=0.62500000 A/G=0.37500000
| Pr(chiSq=0.434,df=1) =0.527 | Genotype Freq. |