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: rs2244012
rs2244012
1 1.000 0.080 5 132565533 intron variant A/G snv 0.33 0.820 1.000 1 2010 2016
dbSNP: rs6871536
rs6871536
2 0.827 0.160 5 132634182 intron variant T/C snv 0.24 0.710 1.000 3 2010 2016
dbSNP: rs2240032
rs2240032
1 1.000 0.080 5 132641435 intron variant C/G;T snv 0.700 1.000 1 2010 2010