Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs747099645
ESR1
0.882 0.120 6 152061061 missense variant C/T snv 1.6E-05 2.8E-05 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
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
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
rs1459132456
SYNE1 ; ESR1
0.925 0.080 6 152125331 missense variant T/C snv 2
rs761843408
SYNE1 ; ESR1
0.925 0.080 6 152125285 synonymous variant A/G snv 3.4E-05 2.8E-05 2
rs139960913
ESR1
1.000 0.080 6 151807928 missense variant C/T snv 3.3E-03 3.1E-03 1