Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2747648
ESR1
0.925 0.080 6 152101200 3 prime UTR variant C/T snv 0.98 2
rs3003925
ESR1
0.925 0.080 6 151963323 intron variant G/A snv 0.80 2
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs523736
ESR1
0.925 0.080 6 151802760 intron variant G/A snv 0.62 2
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs926778
ESR1
0.925 0.080 6 152034647 intron variant C/A snv 0.40 2
rs2881766
ESR1
0.882 0.120 6 151797984 intron variant T/G snv 0.35 5
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs12525163
ESR1
0.925 0.080 6 151719156 intron variant T/C snv 0.27 2
rs2273206
ESR1
0.851 0.280 6 152061176 intron variant G/T snv 0.17 0.22 5
rs2228480
ESR1
0.724 0.360 6 152098960 synonymous variant G/A snv 0.19 0.18 16
rs10484919
ESR1
0.925 0.080 6 151653287 upstream gene variant C/T snv 0.16 2
rs3778609
ESR1
0.925 0.080 6 151812052 intron variant C/T snv 0.13 2
rs9383938
ESR1
0.827 0.160 6 151666222 intron variant G/T snv 0.11 5
rs3798758
ESR1
0.925 0.080 6 152100719 3 prime UTR variant C/A snv 7.4E-02 3
rs746432
ESR1
0.851 0.120 6 151808173 synonymous variant G/A;C snv 6.6E-02 7.0E-02 4
rs9479118
ESR1
0.925 0.080 6 151797989 intron variant T/C snv 1.6E-02 2
rs200075329
ESR1
0.925 0.080 6 151808264 missense variant T/C snv 4.4E-03 4.3E-03 4
rs139960913
ESR1
1.000 0.080 6 151807928 missense variant C/T snv 3.3E-03 3.1E-03 1
rs201145204
ESR1
0.925 0.080 6 151808318 missense variant C/T snv 2.4E-04 1.0E-03 2
rs188957694
ESR1
0.882 0.080 6 151944218 missense variant G/A;C snv 4.0E-05 4.9E-05 6
rs200282497
ESR1
0.925 0.080 6 151944239 missense variant G/C snv 3.6E-05 3.5E-05 4
rs747099645
ESR1
0.882 0.120 6 152061061 missense variant C/T snv 1.6E-05 2.8E-05 3
rs761843408
SYNE1 ; ESR1
0.925 0.080 6 152125285 synonymous variant A/G snv 3.4E-05 2.8E-05 2