>gnl|dbSNP|ss24243565|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
TTCATCCCTG CTCTTCCTGA GCCACGCCAC ATGCACTTGC CCTGCAGAAT GTGGGGCTTA
TGCAGGCCTG ACTGCCTGGG CAGCCAGC
TTCTTTCCTT TA
Y
GACCAGCTGT GG
GACCGTCTGC ATGGGGACAG GGAGCTCATC TCGTCCTCCT GTTGGATATA AACGCGGGAT
CGCTGGTTCC CTGAGTCTTC TGGACATT
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=0.52083331
| C=0.47916666 | C/T=0.54166669 T/T=0.25000000 C/C=0.20833333
| Pr(chiSq=0.174,df=1) =0.752 | Genotype Freq. |
AFD_AFR_PANEL - NORTH AMERICA | 42 | 42 | T=0.90476191
| C=0.09523810 | T/T=0.80952382 C/T=0.19047619
| Pr(chiSq=0.042,df=1) =1.000 | Genotype Freq. |
AFD_CHN_PANEL - NORTH AMERICA | 48 | 48 | T=0.56250000
| C=0.43750000 | C/T=0.70833331 T/T=0.20833333 C/C=0.08333334
| Pr(chiSq=4.629,df=1) =0.050 | Genotype Freq. |