Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs27432
rs27432
1 0.925 0.040 5 96783569 intron variant A/C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs27524
rs27524
1 0.851 0.160 5 96766240 intron variant A/G snv 0.61 0.800 1.000 1 2010 2015
dbSNP: rs151823
rs151823
1 1.000 0.040 5 96824289 intron variant A/C snv 0.90 0.700 1.000 1 2010 2010