>gnl|dbSNP|ss24145263|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
TCACGCAGGC CCAGCTTTGC CCCGACTCCT CGACTTGCTG CGGCCGCCGC CATCCTTGTT
AATATCGAAG TCGCCAATTC CAGGTCTT
CAGGCCAAGT GC
Y
CCGGTCTGAC CA
ACCGCGGACC CTAAAGCCTA GCCCATAGGC TGCATGAGGC AGGGGCGGGG TAAAGCTTGG
CCAATGATAT AAAAGTATTG TAGGACCG
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=0.58333331
| C=0.41666666 | C/T=0.41666666 T/T=0.37500000 C/C=0.20833333
| Pr(chiSq=0.490,df=1) =0.527 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 40 | 40 | T=0.67500001
| C=0.32499999 | C/T=0.55000001 T/T=0.40000001 C/C=0.05000000
| Pr(chiSq=1.286,df=1) =0.273 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | T=0.52083331
| C=0.47916666 | C/T=0.37500000 T/T=0.33333334 C/C=0.29166666
| Pr(chiSq=1.484,df=1) =0.251 | Genotype Freq. |