Source: GWASCAT ×
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: rs1514174
rs1514174
2 1.000 0.080 1 74527379 intron variant C/T snv 0.44 0.800 1.000 1 2013 2013
dbSNP: rs1514177
rs1514177
2 1.000 0.080 1 74525718 intron variant C/G snv 0.49 0.800 1.000 1 2013 2013