Gene: ESR1 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1999805
rs1999805
ESR1
2 1.000 0.120 6 151747229 intron variant G/A snv 0.55 0.800 1.000 3 2008 2009
dbSNP: rs2504063
rs2504063
ESR1 ; LOC107986529
2 6 151769572 intron variant A/G snv 0.50 0.800 1.000 2 2009 2009
dbSNP: rs3020333
rs3020333
ESR1
1 6 151689119 intron variant A/C;G snv 0.800 1.000 2 2009 2018
dbSNP: rs2941740
rs2941740
ESR1
1 6 151688503 intron variant A/G snv 0.40 0.800 1.000 1 2009 2009
dbSNP: rs3020331
rs3020331
ESR1
1 6 151687645 intron variant C/T snv 0.38 0.700 1.000 2 2009 2009
dbSNP: rs11155811
rs11155811
ESR1
1 6 151756711 intron variant C/T snv 0.44 0.700 1.000 1 2009 2009
dbSNP: rs1124674
rs1124674
ESR1
1 6 151759600 intron variant T/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs1293936
rs1293936
ESR1
1 6 151696556 intron variant T/G snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs1336981
rs1336981
ESR1
1 6 151761234 intron variant C/T snv 0.74 0.700 1.000 1 2009 2009
dbSNP: rs1415193
rs1415193
ESR1 ; LOC107986529
1 6 151771503 intron variant T/A snv 0.37 0.700 1.000 1 2009 2009
dbSNP: rs1415194
rs1415194
ESR1
1 6 151742863 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1856057
rs1856057
ESR1
1 6 151746734 intron variant A/G snv 0.55 0.700 1.000 1 2009 2009
dbSNP: rs1890010
rs1890010
ESR1 ; LOC107986529
1 6 151764140 intron variant C/T snv 0.71 0.700 1.000 1 2009 2009
dbSNP: rs1999807
rs1999807
ESR1
1 6 151743064 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs201941147
rs201941147
ESR1
1 6 151735234 intron variant -/A ins 0.700 1.000 1 2009 2009
dbSNP: rs2152750
rs2152750
ESR1
1 6 151749010 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2504065
rs2504065
ESR1
1 6 151774032 intron variant G/A snv 0.47 0.700 1.000 1 2009 2009
dbSNP: rs2504069
rs2504069
ESR1 ; LOC107986529
1 6 151764382 intron variant C/T snv 0.74 0.700 1.000 1 2009 2009
dbSNP: rs2504071
rs2504071
ESR1 ; LOC107986529
1 6 151763727 intron variant T/C snv 0.47 0.700 1.000 1 2009 2009
dbSNP: rs2941741
rs2941741
ESR1
1 6 151687847 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs2982551
rs2982551
ESR1
1 6 151740075 intron variant G/T snv 0.58 0.700 1.000 1 2009 2009
dbSNP: rs2982552
rs2982552
ESR1
1 6 151738428 intron variant G/A snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs2982554
rs2982554
ESR1
1 6 151736875 intron variant A/C snv 0.49 0.700 1.000 1 2009 2009
dbSNP: rs2982556
rs2982556
ESR1
1 6 151735707 intron variant G/A snv 0.46 0.700 1.000 1 2009 2009
dbSNP: rs2982557
rs2982557
ESR1
1 6 151735234 intron variant G/A;T snv 0.700 1.000 1 2009 2009