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: rs3771180
rs3771180
1 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 0.820 1.000 2 2011 2019
dbSNP: rs10197862
rs10197862
2 0.925 0.120 2 102350089 intron variant A/G snv 0.18 0.810 1.000 1 2011 2014
dbSNP: rs13408661
rs13408661
1 1.000 0.080 2 102338622 intron variant G/A snv 0.18 0.810 1.000 1 2011 2012
dbSNP: rs1420101
rs1420101
3 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 0.710 1.000 2 2018 2019
dbSNP: rs72823641
rs72823641
4 0.882 0.080 2 102319699 intron variant T/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs10208293
rs10208293
2 0.882 0.160 2 102349850 intron variant G/A snv 0.33 0.700 1.000 2 2016 2019
dbSNP: rs12470864
rs12470864
4 0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs12479210
rs12479210
1 1.000 0.080 2 102332701 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1861245
rs1861245
2 0.925 0.080 2 102350446 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs3771175
rs3771175
1 0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 0.700 1.000 1 2019 2019