>gnl|dbSNP|ss23803635|allelePos=101|len=201|taxid=9606|alleles='A/G'|mol=Genomic
TGGTGGCTGC AGTGAGCCGA GATCGCACCA CTGCACTCCA GCCTGGGCAA CAGAGCCAGA
CTCCATTTAA AAAAAGAAAA GCAGGTGA
GGACGTGTGA GC
R
AGTCTGGGCC AT
GCTGCCAAGC TCCCGCTTCT CCGAGCAGCT CCACACAAGG AGCAGAGGCA GCTCCAGTTC
CACAGCCAGA CACAGTCATT TTCCCTCT
Population ID -Class | Total Sample (2N) | Founder (2N) | Major Allele Freq. | Minor Allele Freq. | Genotype Freq. | HWE Goodness of Fit | Data Source | AFD_CHN_PANEL - NORTH AMERICA | 32 | 32 | G=0.87500000
| A=0.12500000 | G/G=0.81250000 A/G=0.12500000 A/A=0.06250000
| Pr(chiSq=2.939,df=1) =0.100 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 42 | 42 | A=0.57142860
| G=0.42857143 | A/G=0.38095239 A/A=0.38095239 G/G=0.23809524
| Pr(chiSq=1.037,df=1) =0.317 | Genotype Freq. |
AFD_EUR_PANEL - NORTH AMERICA | 46 | 46 | G=0.73913044
| A=0.26086956 | G/G=0.56521738 A/G=0.34782609 A/A=0.08695652
| Pr(chiSq=0.221,df=1) =0.655 | Genotype Freq. |