There are ~100 SNPs associated with RA at genome wide significance.
If you enter in just the SNP ID into pubmed, you can sometimes find links to other papers describing a functional effect of the variant.
Individually submitting 100 requests is tedious, so I thought there is probably a "batch submit" button Entrez or EUtilz tool to do this.
However, I was not able to get what options I could find to work. Batch Entrez - NCBI, unless I am mistaken, does not allow you to go from rsID list --> citation list. Instead, what I am looking for is something like dbSNP Batch Query, but that hits the pubmed dbase instead of dbSNP.
How might one submit a list of the form
rs12140275 rs2476601 rs624988 rs2228145 rs2317230 rs4656942 ....
and receive back a flat file, or webpage, etc. containing the title and URL of each study? If I had that, I could scan through very quickly. Thanks in advance.