>gnl|dbSNP|ss24243583|allelePos=101|len=201|taxid=9606|alleles='A/C'|mol=Genomic
CTGCTGCTGT GGCTGTGTAA AGAAGTCCCG ATTCCGAAAG CTCCGACGGG AACATTTACA
GATGCAACAA CGTGCTGTCT GGGTTGGC
TTCAACATTA CA
M
GAGAGGGGAG CA
CGTGGGGGCA CGGGAGAAAC AAGACGGGCT GAGTTGCTAG TTGCGCAAGC TCAGTGACCG
TGACAAGGGA GAGTCCTGAG GGTTTCTG
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 | 44 | 44 | C=0.54545456
| A=0.45454547 | A/C=0.54545456 C/C=0.27272728 A/A=0.18181819
| Pr(chiSq=0.220,df=1) =0.655 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 40 | 40 | C=0.97500002
| A=0.02500000 | C/C=0.94999999 A/C=0.05000000
| Pr(chiSq=0.001,df=1) =1.000 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 44 | 44 | C=0.72727275
| A=0.27272728 | C/C=0.50000000 A/C=0.45454547 A/A=0.04545455
| Pr(chiSq=0.468,df=1) =0.527 | Genotype Freq. |