>gnl|dbSNP|ss24237297|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
CCCTGTGCAG AAAGAGTCCT GGGTCCTCCG TCCTCTTCCA ACCTCCTGCT GAGAGTCCCA
GGCAAGCACA GATTCCCAGG CTGGGGTA
TCCCATCCAG AC
Y
TTCGCCCTCT GT
ACCCTTCGTG CTGGGCCTGG GGTGGAGTGT ACTTGGAGGG GACCCATCCT CAATCCACCT
CGTTCCGGAG AGCTGAGCCC TCAAGAAG
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 | T=0.62500000
| C=0.37500000 | C/T=0.50000000 T/T=0.37500000 C/C=0.12500000
| Pr(chiSq=0.107,df=1) =0.752 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | T=0.71739131
| C=0.28260869 | C/T=0.47826087 T/T=0.47826087 C/C=0.04347826
| Pr(chiSq=0.741,df=1) =0.403 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | T=0.66666669
| C=0.33333334 | T/T=0.45833334 C/T=0.41666666 C/C=0.12500000
| Pr(chiSq=0.094,df=1) =1.000 | Genotype Freq. |