Minor Allele Frequency (MAF) found in the population diversity section of the refSNP report is very high in SNPs from different sets of samples from the same ethnicity. Why?
Rs6523677 is annotated as “A” in the reference sequences, but the genotyping (HapMap) of 300 individuals shows a “C” for all alleles. It's very unlikely that genotyping of any 300 individuals will show a “C” allele 300 times. More.
I cant really gove you an answer,but what I can give you is a way to a solution, that is you have to find the anglde that you relate to or peaks your interest. A good paper is one that people get drawn into because it reaches them ln some way.As for me WW11 to me, I think of the holocaust and the effect it had on the survivors, their families and those who stood by and did nothing until it was too late.
Related Questions
Which tables and columns in the schema contain the data found in the Population Diversity section of the refSNP Cluster Report?
What is the reference database for the ADT (e.g., source and version for sequence, Minor Allele Frequency [MAF], validation)?
I’ve submitted millions of mouse SNPs, and have their submitted (ss) numbers — how do I check to see if they have refSNP (rs) numbers yet?
How do I get the chromosome, chromosome position, alleles and Ancestral allele for each SNP in a file of refSNP numbers I obtained from HapMap?
Why are four nucleotides listed for the average allele frequency of rs702424?
How do I access the legend for the icons in the SNP validation section of the refSNP (rs) and submitted SNP (ss) reports?