Gene: RGS22 ×
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: rs7006527
rs7006527
RGS22
4 0.851 0.040 8 100012277 intron variant A/C;T snv 0.700 1.000 2 2014 2015
dbSNP: rs141115006
rs141115006
RGS22
3 0.882 0.040 8 99992792 intron variant C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs2199333
rs2199333
RGS22
3 0.882 0.040 8 99999120 intron variant C/G;T snv 0.700 1.000 1 2019 2019