Gene: RGS9 ×
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: rs1122079
rs1122079
RGS9
1 1.000 0.080 17 65218385 intron variant A/C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1530351
rs1530351
RGS9
2 0.925 0.080 17 65135491 intron variant G/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs2292592
rs2292592
RGS9
1 1.000 0.080 17 65208091 intron variant A/G snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs2292593
rs2292593
RGS9
1 1.000 0.080 17 65201802 intron variant T/C snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs2869577
rs2869577
RGS9
1 1.000 0.080 17 65199474 intron variant C/G snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs4791230
rs4791230
RGS9
2 0.925 0.080 17 65136210 intron variant C/T snv 0.75 0.010 1.000 1 2015 2015
dbSNP: rs8070231
rs8070231
RGS9
1 1.000 0.080 17 65198827 intron variant A/G snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs8077696
rs8077696
RGS9
1 1.000 0.080 17 65196443 intron variant C/A snv 0.19 0.010 1.000 1 2015 2015
dbSNP: rs9916525
rs9916525
RGS9
1 1.000 0.080 17 65215319 intron variant C/T snv 0.42 0.010 1.000 1 2015 2015