>gnl|dbSNP|ss24398124|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
AAGCTCCGAG CTCAGCAGAT CCATTAGGGG TGCCAAACAA ACCCTCCTCA CAGCCCCTCA
CACTCTACCG CAGCCGGCCG GGATGCCC
ACCTTGTGCT GC
Y
GCGTCTCCGG AT
GATCTTGGTG CGGCTCTTCA CTTTGTAAGC CGAGAGCGGG GTCTCCCCAG AGAGGGGCTT
CAAGCCACTG TGTCCTACTG CTGGTCTG
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 | 46 | 46 | C=0.69565219
| T=0.30434781 | C/C=0.47826087 C/T=0.43478259 T/T=0.08695652
| Pr(chiSq=0.017,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | C=0.76086956
| T=0.23913044 | C/C=0.60869563 C/T=0.30434781 T/T=0.08695652
| Pr(chiSq=0.616,df=1) =0.439 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 46 | 46 | C=0.93478262
| T=0.06521739 | C/C=0.86956519 C/T=0.13043478
| Pr(chiSq=0.014,df=1) =1.000 | Genotype Freq. |