>gnl|dbSNP|ss24309656|allelePos=101|len=201|taxid=9606|alleles='C/G'|mol=Genomic
CCGTGTGTTT TTTAAAGTGT GTCTGCCTCT GAATCTCCCT GGCTCTGCTC ATCTCAGAAG
GTCCCTGGAG GAGGGCTCAT GGCTGACA
CATGTTAGCA TA
S
GAGAAGGGGA AG
AATTTTATTT ATCTGCCACT AATCCCCATG TGTCTCATAC CCAAATCTAG GATTTTCCTC
TTCCCACCTG GAGTATCCGG CGTGCATG
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 | C=0.54166669
| G=0.45833334 | C/G=0.50000000 C/C=0.29166666 G/G=0.20833333
| Pr(chiSq=0.001,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | C=0.63043481
| G=0.36956522 | C/G=0.56521738 C/C=0.34782609 G/G=0.08695652
| Pr(chiSq=1.043,df=1) =0.317 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.68750000
| G=0.31250000 | C/G=0.54166669 C/C=0.41666666 G/G=0.04166667
| Pr(chiSq=1.630,df=1) =0.251 | Genotype Freq. |