>gnl|dbSNP|ss23967789|allelePos=101|len=201|taxid=9606|alleles='A/G'|mol=Genomic
GTCTGAACAC TTCTTCCAGG TCCAAGATGG TAATGGGTAT CCATCCGAGA AACAGGACGC
CTGACTTGCC GATGCTTCTG CGAGCACT
TGAGGTTTCC CT
R
TAGAAAAGAA CG
TGTGAAATAA GCTCACTGGC TGGGCATAGT GGTTCACTCC TATAATACCA ATACTTTGTG
AAGCCAAGGT GGGAGGATCA CTTGGGCC
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=0.85416669
| A=0.14583333 | G/G=0.75000000 A/G=0.20833333 A/A=0.04166667
| Pr(chiSq=0.644,df=1) =0.439 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | A=0.73913044
| G=0.26086956 | A/A=0.56521738 A/G=0.34782609 G/G=0.08695652
| Pr(chiSq=0.221,df=1) =0.655 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | G=0.68750000
| A=0.31250000 | A/G=0.45833334 G/G=0.45833334 A/A=0.08333334
| Pr(chiSq=0.107,df=1) =0.752 | Genotype Freq. |