>gnl|dbSNP|ss24491020|allelePos=101|len=201|taxid=9606|alleles='G/A'|mol=Genomic
TGCAGGGGGC AACTGTGAGT GGGCAGGGCT CCCGCTGCAC AGCTTCCTCC CTCCCCGGGC
ACGCCAGGGA CCTCACCATG GCACACAC
CACTCTGCTG AC
R
TAGACGGGGC TT
CCCCGCAGAG CACAGTCTGT GGCTGGGTCA GTCTGGAAGT GCAGGCTCTT GTCTAGCAGC
TTCAGGCAGA TGTCTATGAT TTTGTCTT
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=0.62500000
| A=0.37500000 | A/G=0.50000000 G/G=0.37500000 A/A=0.12500000
| Pr(chiSq=0.107,df=1) =0.752 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 40 | 40 | A=0.69999999
| G=0.30000001 | A/G=0.50000000 A/A=0.44999999 G/G=0.05000000
| Pr(chiSq=0.726,df=1) =0.403 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 44 | 44 | G=0.75000000
| A=0.25000000 | G/G=0.59090906 A/G=0.31818181 A/A=0.09090909
| Pr(chiSq=0.505,df=1) =0.479 | Genotype Freq. |