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: rs2941504
rs2941504
1 1.000 0.080 17 39674647 synonymous variant A/G snv 0.67 0.64 0.710 1.000 1 2010 2011
dbSNP: rs12150298
rs12150298
1 1.000 0.080 17 39678288 intron variant T/C snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs1565922
rs1565922
1 1.000 0.080 17 39674782 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2517955
rs2517955
1 1.000 0.080 17 39687428 intron variant C/T snv 0.51 0.700 1.000 1 2011 2011
dbSNP: rs2941503
rs2941503
1 1.000 0.080 17 39672492 missense variant A/G snv 0.64 0.700 1.000 1 2010 2010