Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs762292600
ESR1
0.925 0.080 6 151944316 missense variant A/G snv 4.0E-06 1.4E-05 7
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
rs1062577
ESR1
0.882 0.080 6 152102770 3 prime UTR variant T/A;G snv 4
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
rs3798758
ESR1
0.925 0.080 6 152100719 3 prime UTR variant C/A snv 7.4E-02 3
rs767863538
ESR1
0.925 0.080 6 151808207 missense variant C/G;T snv 5.6E-06; 5.6E-06 3
rs10484919
ESR1
0.925 0.080 6 151653287 upstream gene variant C/T snv 0.16 2
rs12525163
ESR1
0.925 0.080 6 151719156 intron variant T/C snv 0.27 2
rs1459132456
SYNE1 ; ESR1
0.925 0.080 6 152125331 missense variant T/C snv 2
rs201145204
ESR1
0.925 0.080 6 151808318 missense variant C/T snv 2.4E-04 1.0E-03 2
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
rs3778609
ESR1
0.925 0.080 6 151812052 intron variant C/T snv 0.13 2
rs523736
ESR1
0.925 0.080 6 151802760 intron variant G/A snv 0.62 2
rs760503206
ESR1
0.925 0.080 6 151807956 missense variant T/C snv 4.0E-06 2
rs761843408
SYNE1 ; ESR1
0.925 0.080 6 152125285 synonymous variant A/G snv 3.4E-05 2.8E-05 2
rs7766585
ESR1
0.925 0.080 6 152074901 intron variant T/A;G snv 2
rs926778
ESR1
0.925 0.080 6 152034647 intron variant C/A snv 0.40 2
rs9479118
ESR1
0.925 0.080 6 151797989 intron variant T/C snv 1.6E-02 2