>gnl|dbSNP|ss24243614|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
TTATAGAAAT TATTTTCAAA ATTTTAGTAA GCAGTTTGAT GTGAGCTCTA AAACGATTAT
ACAAGTAAAA AGGTAGCATG TTTTCCAT
TCAGCTGGGA GA
Y
GGCTGAGGTG CA
GCAGGCGTGC AGTGATACTT GCTGAATGGA CAGAAGCCGT TCCCACATGG AGCTTCCATG
ACATGCATTT ACACACCCCG ATTCTTTA
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=0.54166669
| C=0.45833334 | C/T=0.41666666 T/T=0.33333334 C/C=0.25000000
| Pr(chiSq=0.621,df=1) =0.439 | 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 | 48 | 48 | T=0.97916669
| C=0.02083333 | T/T=0.95833331 C/T=0.04166667
| Pr(chiSq=0.000,df=1) =1.000 | Genotype Freq. |