>gnl|dbSNP|ss66859656|allelePos=101|len=201|taxid=9606|alleles='G/C'|mol=Genomic
TGAAGATAAG GCTCTAGAAG ACAGGAGACC ATATAAATGC AAATTTTGAA AAATTATTGC
AATRTCCTAT TCCTTTCCTG AAACCAAAAA GCAATGATTA
S
TATATGTTTG TACATTCATT CNTTCTTTTT TTTTAACAAA CTTGATTAAG TAACATTTTT
TAGAATACAG TCTTCAAASA GCTTACAATT TAGTTGAATG
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 | 52 | 52 | C=0.65384614
| G=0.34615386 | C/C=0.46153846 C/G=0.38461539 G/G=0.15384616
| Pr(chiSq=0.588,df=1) =0.479 | Genotype Freq. |
CEU_GENO_PANEL | 68 | 68 | C=0.83823532
| G=0.16176471 | C/C=0.70588237 C/G=0.26470590 G/G=0.02941176
| Pr(chiSq=0.019,df=1) =1.000 | Genotype Freq. |
AAM_GENO_PANEL | 118 | 118 | C=0.70338982
| G=0.29661018 | C/C=0.47457626 C/G=0.45762712 G/G=0.06779661
| Pr(chiSq=0.552,df=1) =0.479 | Genotype Freq. |
CHB_GENO_PANEL | 90 | 90 | C=0.87777776
| G=0.12222222 | C/C=0.80000001 C/G=0.15555556 G/G=0.04444445
| Pr(chiSq=3.404,df=1) =0.100 | Genotype Freq. |
YRI_GENO_PANEL | 112 | 112 | C=0.58928573
| G=0.41071430 | C/G=0.42857143 C/C=0.37500000 G/G=0.19642857
| Pr(chiSq=0.736,df=1) =0.403 | Genotype Freq. |