>gnl|dbSNP|ss23145056|allelePos=101|len=201|taxid=9606|alleles='G/A'|mol=Genomic
TTTTCTCTTT TCTGAGTGAA AATGCTGAAT GCAGTTCCTC TAGAAAAAAA TGCTTAACTT
TCTGTCAACC TTCTGGTTTC CTTAGAGG
ATTTGGTACA AC
R
TAGAAATGTG AT
TGGCGATGTC TATTCTCAGG GGCCTGCCTC TCCTTTTGAA ATAAACAATG GGTTAGGCAG
TCCCCTGAAG TATACAGGTA CCACTGAA
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 | A=0.75000000
| G=0.25000000 | A/A=0.62500000 A/G=0.25000000 G/G=0.12500000
| Pr(chiSq=2.667,df=1) =0.150 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 42 | 42 | A=0.57142860
| G=0.42857143 | A/G=0.47619048 A/A=0.33333334 G/G=0.19047619
| Pr(chiSq=0.016,df=1) =1.000 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | A=0.77083331
| G=0.22916667 | A/A=0.58333331 A/G=0.37500000 G/G=0.04166667
| Pr(chiSq=0.091,df=1) =1.000 | Genotype Freq. |