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: rs10267578
rs10267578
1 1.000 0.040 7 50134961 intron variant C/T snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs10411970
rs10411970
1 1.000 0.040 19 4814636 downstream gene variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10817678
rs10817678
1 1.000 0.040 9 114817177 intergenic variant G/A snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs11204668
rs11204668
1 1.000 0.040 1 150571210 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs115062572
rs115062572
1 1.000 0.040 6 31895099 intron variant C/T snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs116295688
rs116295688
1 1.000 0.040 3 159545173 intron variant G/T snv 2.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs11649485
rs11649485
1 1.000 0.040 16 85980849 intron variant A/G snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs11684030
rs11684030
1 1.000 0.040 2 191152153 upstream gene variant G/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs11710258
rs11710258
1 1.000 0.040 3 159551353 intron variant A/G snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs11757201
rs11757201
5 0.851 0.040 6 137682685 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11928736
rs11928736
1 1.000 0.040 3 159847620 intron variant G/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs11989430
rs11989430
1 1.000 0.040 8 89806387 regulatory region variant A/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs12232497
rs12232497
15 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs12629300
rs12629300
LTF
1 1.000 0.040 3 46442045 intron variant A/T snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs1353248
rs1353248
2 0.925 0.120 3 159905770 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs138753323
rs138753323
1 1.000 0.040 6 32205822 intron variant T/C snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs142628781
rs142628781
1 1.000 0.040 6 31303021 intron variant C/T snv 3.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs144474740
rs144474740
1 1.000 0.040 19 18584880 intron variant C/T snv 4.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs145743887
rs145743887
1 1.000 0.040 3 159464380 intron variant A/T snv 9.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs145925847
rs145925847
1 1.000 0.040 3 160337849 intron variant T/A snv 7.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs1491958
rs1491958
1 1.000 0.040 3 46081389 intergenic variant C/T snv 6.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs150383292
rs150383292
1 1.000 0.040 3 161562034 intergenic variant C/T snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs150921465
rs150921465
1 1.000 0.040 3 159518731 intron variant G/A;T snv 9.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs1545536
rs1545536
1 1.000 0.040 8 143560999 splice region variant C/A;G;T snv 4.0E-06; 0.26 0.700 1.000 1 2019 2019
dbSNP: rs16823566
rs16823566
1 1.000 0.040 2 144192681 intron variant G/T snv 0.14 0.700 1.000 1 2019 2019