>gnl|dbSNP|ss23842786|allelePos=101|len=201|taxid=9606|alleles='G/C'|mol=Genomic
TGGCGTCTGT GCTGAGGATC TGGCTGGCCC GCTTAGATCG GAAGTAGTTG CTGGCAATGT
TTTCACTGTT GCTCCGACTG AGCATGAG
CCTGTAGCGG TC
S
TCCTCCTGCC GA
GATGCAGATG CCCGTGGTCA CGTCCCCTTG TTTGTGCCCC TGGCACAGGG CTCCACAGCC
TCTGGTATCC TGGGGCAGTG GGGGCCGC
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 | C=0.79166669
| G=0.20833333 | C/C=0.62500000 C/G=0.33333334 G/G=0.04166667
| Pr(chiSq=0.003,df=1) =1.000 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 46 | 46 | C=0.71739131
| G=0.28260869 | C/G=0.56521738 C/C=0.43478259
| Pr(chiSq=1.732,df=1) =0.200 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.64583331
| G=0.35416666 | C/G=0.45833334 C/C=0.41666666 G/G=0.12500000
| Pr(chiSq=0.000,df=1) =1.000 | Genotype Freq. |