>gnl|dbSNP|ss66858970|allelePos=101|len=201|taxid=9606|alleles='A/G'|mol=Genomic
GTGGGCTTCA TCCTCACCTA TAGAAAATTC AATTATAAAG ACAATACAGA TCTGGTCGAG
TTTAAAACTC TCACTGAGGA AGAGGTTGAA GAAGTGCTGA
R
AAATATATTT AAGATTTCCT TGGGGAGAAA TCTCGTGCCC AAACCTGGTG ATGRATCCCT
TACTATTTAG AATAAGGAAC AAAATAAACC CTTGTGTATG
Population ID -Class | Total Sample (2N) | Founder (2N) | Major Allele Freq. | Minor Allele Freq. | Genotype Freq. | HWE Goodness of Fit | Data Source | HSP_GENO_PANEL | 54 | 54 | A=0.53703701
| G=0.46296296 | A/G=0.48148149 A/A=0.29629630 G/G=0.22222222
| Pr(chiSq=0.027,df=1) =1.000 | Genotype Freq. |
CEU_GENO_PANEL | 68 | 68 | A=0.51470590
| G=0.48529410 | A/G=0.55882353 A/A=0.23529412 G/G=0.20588236
| Pr(chiSq=0.478,df=1) =0.527 | Genotype Freq. |
AAM_GENO_PANEL | 122 | 122 | A=0.68032789
| G=0.31967214 | A/A=0.49180329 A/G=0.37704918 G/G=0.13114753
| Pr(chiSq=1.081,df=1) =0.317 | Genotype Freq. |
CHB_GENO_PANEL | 90 | 90 | A=0.97777778
| G=0.02222222 | A/A=0.95555556 A/G=0.04444445
| Pr(chiSq=0.001,df=1) =1.000 | Genotype Freq. |
YRI_GENO_PANEL | 120 | 120 | A=0.58333331
| G=0.41666666 | A/G=0.50000000 A/A=0.33333334 G/G=0.16666667
| Pr(chiSq=0.049,df=1) =1.000 | Genotype Freq. |