Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs2228480
ESR1
0.724 0.360 6 152098960 synonymous variant G/A snv 0.19 0.18 16
rs2077647
ESR1
0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs3020314
ESR1
0.790 0.280 6 151949537 intron variant C/G;T snv 7
rs200960801
ESR1
0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6
rs9383938
ESR1
0.827 0.160 6 151666222 intron variant G/T snv 0.11 5
rs2273206
ESR1
0.851 0.280 6 152061176 intron variant G/T snv 0.17 0.22 5
rs757200716
ESR1
0.851 0.160 6 151842617 missense variant G/A snv 8.0E-06 5
rs746432
ESR1
0.851 0.120 6 151808173 synonymous variant G/A;C snv 6.6E-02 7.0E-02 4
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs188957694
ESR1
0.882 0.080 6 151944218 missense variant G/A;C snv 4.0E-05 4.9E-05 6
rs1462893414
ESR1
0.882 0.080 6 151944323 missense variant A/G snv 4.0E-06 7.0E-06 5
rs2881766
ESR1
0.882 0.120 6 151797984 intron variant T/G snv 0.35 5
rs1062577
ESR1
0.882 0.080 6 152102770 3 prime UTR variant T/A;G snv 4
rs1455751791
ESR1
0.882 0.120 6 152011735 synonymous variant C/G snv 4.0E-06 3
rs747099645
ESR1
0.882 0.120 6 152061061 missense variant C/T snv 1.6E-05 2.8E-05 3
rs762292600
ESR1
0.925 0.080 6 151944316 missense variant A/G snv 4.0E-06 1.4E-05 7
rs1364963022
ESR1
0.925 0.080 6 151944233 missense variant G/C snv 4.0E-06 4
rs200075329
ESR1
0.925 0.080 6 151808264 missense variant T/C snv 4.4E-03 4.3E-03 4
rs200282497
ESR1
0.925 0.080 6 151944239 missense variant G/C snv 3.6E-05 3.5E-05 4
rs2144025
ESR1
0.925 0.080 6 151986571 intron variant T/A;C snv 4
rs1207112399
ESR1
0.925 0.080 6 151842614 missense variant G/A snv 4.0E-06 7.0E-06 3