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: rs1058808
rs1058808
1 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 0.710 1.000 1 2011 2013
dbSNP: rs1810132
rs1810132
1 1.000 0.080 17 39709752 intron variant C/T snv 0.64 0.700 1.000 2 2010 2011
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: rs2952155
rs2952155
1 1.000 0.080 17 39705465 intron variant T/C;G snv 0.700 1.000 1 2011 2011