>gnl|dbSNP|ss23160617|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
TTCCCGCTGA AACTAACTTA ATTCTACCTA ATTTGCGTGG GGAGTAGTTG GCCAAATCAT
CAAATTGTTA ACTTTTTGCT AACATATT
GTGTAATCAA CC
Y
TAGGTGTTAA AA
AAGGTTTGCT TGTTTCTTTC ATGCAAATAC TAATGTAGCC CTTTTTTCTT AGCGTATAGC
TTCTGGCCTG GGCTTGGCCT GGATTGTT
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=0.86956519
| T=0.13043478 | C/C=0.78260869 C/T=0.17391305 T/T=0.04347826
| Pr(chiSq=1.252,df=1) =0.273 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 44 | 44 | C=0.61363637
| T=0.38636363 | C/T=0.59090906 C/C=0.31818181 T/T=0.09090909
| Pr(chiSq=1.333,df=1) =0.251 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 46 | 46 | T=0.71739131
| C=0.28260869 | T/T=0.52173913 C/T=0.39130434 C/C=0.08695652
| Pr(chiSq=0.028,df=1) =1.000 | Genotype Freq. |