Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1206642175
ESR1
0.925 0.080 6 151808263 synonymous variant G/A snv 7.0E-06 3
rs767863538
ESR1
0.925 0.080 6 151808207 missense variant C/G;T snv 5.6E-06; 5.6E-06 3
rs747099645
ESR1
0.882 0.120 6 152061061 missense variant C/T snv 1.6E-05 2.8E-05 3
rs1455751791
ESR1
0.882 0.120 6 152011735 synonymous variant C/G snv 4.0E-06 3
rs1207112399
ESR1
0.925 0.080 6 151842614 missense variant G/A snv 4.0E-06 7.0E-06 3
rs6932902
ESR1
0.882 0.160 6 152055389 intron variant G/A snv 0.22 3
rs9397456
ESR1
0.882 0.160 6 151926017 intron variant A/G;T snv 3
rs1709183
ESR1
0.882 0.160 6 151872861 intron variant C/T snv 0.67 3
rs1033182
ESR1
0.882 0.160 6 151873899 intron variant G/A snv 0.26 3
rs2431260
ESR1
0.882 0.160 6 151871196 intron variant G/C;T snv 3
rs766779326
ESR1
1.000 0.040 6 151944344 missense variant C/T snv 4.0E-06 7.0E-06 2
rs2207396
ESR1
0.925 0.120 6 152061247 intron variant G/A snv 0.23 2
rs760503206
ESR1
0.925 0.080 6 151807956 missense variant T/C snv 4.0E-06 2
rs9479118
ESR1
0.925 0.080 6 151797989 intron variant T/C snv 1.6E-02 2
rs201145204
ESR1
0.925 0.080 6 151808318 missense variant C/T snv 2.4E-04 1.0E-03 2
rs3003925
ESR1
0.925 0.080 6 151963323 intron variant G/A snv 0.80 2
rs7766585
ESR1
0.925 0.080 6 152074901 intron variant T/A;G snv 2
rs523736
ESR1
0.925 0.080 6 151802760 intron variant G/A snv 0.62 2
rs3778609
ESR1
0.925 0.080 6 151812052 intron variant C/T snv 0.13 2
rs3798758
ESR1
0.925 0.080 6 152100719 3 prime UTR variant C/A snv 7.4E-02 2
rs12525163
ESR1
0.925 0.080 6 151719156 intron variant T/C snv 0.27 2
rs10484919
ESR1
0.925 0.080 6 151653287 upstream gene variant C/T snv 0.16 2
rs2747648
ESR1
0.925 0.080 6 152101200 3 prime UTR variant C/T snv 0.98 2
rs926778
ESR1
0.925 0.080 6 152034647 intron variant C/A snv 0.40 2
rs772596249
ESR1
6 151842724 missense variant G/A snv 4.0E-06 2