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: rs3184504
rs3184504
24 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 0.800 1.000 1 2012 2019
dbSNP: rs477515
rs477515
7 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs4915076
rs4915076
1 0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs4915077
rs4915077
1 1.000 0.040 1 107823394 intron variant T/C snv 9.0E-02 0.800 1.000 1 2012 2012
dbSNP: rs653178
rs653178
17 0.672 0.600 12 111569952 intron variant C/T snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs6679677
rs6679677
6 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 0.800 1.000 1 2012 2012
dbSNP: rs7024345
rs7024345
2 0.925 0.080 9 97832956 intron variant A/G snv 0.82 0.700 1.000 1 2012 2012
dbSNP: rs7848973
rs7848973
2 0.925 0.080 9 97826557 intron variant A/G snv 0.67 0.700 1.000 1 2012 2012
dbSNP: rs7850258
rs7850258
3 0.827 0.200 9 97786731 intron variant A/G snv 0.72 0.820 1.000 2 2011 2019
dbSNP: rs7866436
rs7866436
2 0.925 0.080 9 97887814 intergenic variant G/A snv 0.70 0.700 1.000 1 2012 2012
dbSNP: rs907580
rs907580
2 0.851 0.080 9 97860315 downstream gene variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs925487
rs925487
2 0.925 0.080 9 97874116 regulatory region variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs925489
rs925489
5 0.882 0.080 9 97784318 intron variant C/T snv 0.71 0.800 1.000 2 2011 2012
dbSNP: rs9262638
rs9262638
1 1.000 0.040 6 31058212 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9262639
rs9262639
1 1.000 0.040 6 31058232 intron variant C/T snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs948426
rs948426
1 1.000 0.040 18 6567183 intron variant A/G snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs965513
rs965513
4 0.742 0.200 9 97793827 intron variant A/G;T snv 0.700 1.000 2 2011 2012