Description
The NCBI ALlele Frequency Aggregator (ALFA) pipeline is developed to compute allele frequency for variants in dbGaP across approved un-restricted studies and to provide the data as open-access to the public through dbSNP. The goal of the ALFA project is to make frequency data from over 1M dbGaP subjects open-access in future releases to facilitate discoveries and interpretations of common and rare variants with biological impacts or causing diseases.
The R4 release of 408,709 subjects included allele counts and frequency for 15.5 million rs site including 959,966 ClinVar RS IDs. More information about ALFA can be found at https://www.ncbi.nlm.nih.gov/snp/docs/gsr/alfa/ and any questions about ALFA track data should be forwarded to <mailto:snp-admin@ncbi.nlm.nih.gov>.
Subtracks
This track contains data from 12 populations:
* ALFA data for African population
* ALFA data for African American population
* ALFA data for African Others population
* ALFA data for Asian population
* ALFA data for East Asian population
* ALFA data for European population
* ALFA data for Global population
* ALFA data for Latin American 1 population
* ALFA data for Latin American 2 population
* ALFA data for Other population
* ALFA data for Other Asian population
* ALFA data for South Asian population
The variant label is the dbSNP reference SNP ID (rsid).
The mouseover (displayed when the mouse is hovered over a variant) shows the following:
The detail page contains the following:
The colors indicate the alternate allele frequencies.