Gene: RGS2 ×
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: rs4606
rs4606
RGS2
16 0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 0.040 1.000 4 2013 2018
dbSNP: rs200339834
rs200339834
RGS2
1 1 192810186 missense variant G/A snv 1.2E-04 7.0E-05 0.020 1.000 2 2005 2008
dbSNP: rs2746071
rs2746071
RGS2
4 0.882 0.160 1 192808434 intron variant A/G snv 0.35 0.010 1.000 1 2014 2014
dbSNP: rs34717272
rs34717272
RGS2
1 1 192810962 intron variant TC/CT mnv 0.010 1.000 1 2008 2008
dbSNP: rs74466425
rs74466425
RGS2
1 1 192809125 missense variant G/C snv 3.0E-04 2.0E-04 0.010 1.000 1 2010 2010
dbSNP: rs77790369
rs77790369
RGS2
1 1 192811493 missense variant A/G snv 1.6E-05 0.010 1.000 1 2010 2010