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: rs1023945
rs1023945
2 0.925 0.120 1 145731972 intron variant G/A snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs1471628
rs1471628
2 0.925 0.120 1 145728029 intron variant A/T snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs2231375
rs2231375
2 0.925 0.120 1 145738392 3 prime UTR variant C/T snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs4970874
rs4970874
2 0.925 0.120 1 145725691 intron variant A/G snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs744877
rs744877
2 0.882 0.200 1 145720709 intron variant C/A snv 0.47 0.700 1.000 1 2013 2013
dbSNP: rs9728526
rs9728526
2 0.925 0.120 1 145718303 upstream gene variant C/T snv 0.50 0.700 1.000 1 2013 2013