>gnl|dbSNP|ss66856878|allelePos=101|len=201|taxid=9606|alleles='A/G'|mol=Genomic
TTTCGRCATA GTGTGGTGGT GCCCTATGAG CCGCCTGAGG TCTGGTTTGC AACTGGGGTC
TCTGGGAGGA GGGGTTAAGG GTGGTTRTCA GTGGCCCTCC
R
GGTGAGCAGT AGGGGGGCTT TCTCCTGCTG CTTATTTGAC CTCCCTATAA CCCCATGAGA
TGTGCAAAGT AAATGGGTTT AACTATTGCA CAGTTGAAAA
Population ID
-Class | Total
Sample
(2N) | Founder
(2N) | Major
Allele
Freq. | Minor
Allele
Freq. | Genotype
Freq. | HWE Goodness of Fit | Data
Source | | HSP_GENO_PANEL | 116 | 116 | G=0.91379309
| A=0.08620690 | G/G=0.84482759
A/G=0.13793103
A/A=0.01724138
| Pr(chiSq=0.899,df=1)
=0.371 | Genotype
Freq. |
| CEU_GENO_PANEL | 118 | 118 | G=0.90677965
| A=0.09322034 | G/G=0.81355929
A/G=0.18644068
| Pr(chiSq=0.111,df=1)
=0.752 | Genotype
Freq. |
| AAM_GENO_PANEL | 124 | 124 | G=0.78225809
| A=0.21774194 | G/G=0.62903225
A/G=0.30645162
A/A=0.06451613
| Pr(chiSq=0.625,df=1)
=0.439 | Genotype
Freq. |
| CHB_GENO_PANEL | 88 | 88 | G=0.96590906
| A=0.03409091 | G/G=0.93181819
A/G=0.06818182
| Pr(chiSq=0.004,df=1)
=1.000 | Genotype
Freq. |
| YRI_GENO_PANEL | 120 | 120 | G=0.69999999
| A=0.30000001 | G/G=0.51666665
A/G=0.36666667
A/A=0.11666667
| Pr(chiSq=0.967,df=1)
=0.343 | Genotype
Freq. |
