>gnl|dbSNP|ss24235117|allelePos=101|len=201|taxid=9606|alleles='C/G'|mol=Genomic
TTGTTGCAAG ATGGAAGATG TACAGAAGGC AGGTGCAGAG GCTTCCTGCT AAGGCCTGTG
GCTGTCAGAA GAGCAGTTGG TGGCCAGG
AGAGCAGCAT AC
S
TCAAGGAGGG TG
AGGCAACTGG ATGGTTAGGG AGATGGAATG ACTAGAAGCA GCTGCAATGA GAAAAAGGGC
TTAAGGGGAA TTTTAGGCAG TTTTCCTA
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=0.87500000
| G=0.12500000 | C/C=0.79166669 C/G=0.16666667 G/G=0.04166667
| Pr(chiSq=1.361,df=1) =0.251 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 44 | 44 | C=0.97727275
| G=0.02272727 | C/C=0.95454544 C/G=0.04545455
| Pr(chiSq=0.001,df=1) =1.000 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | C=0.97916669
| G=0.02083333 | C/C=0.95833331 C/G=0.04166667
| Pr(chiSq=0.000,df=1) =1.000 | Genotype Freq. |