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: rs121908449
rs121908449
RGS9
2 1.000 0.040 17 65197160 missense variant T/C snv 1.2E-04 1.8E-04 0.800 1.000 1 2004 2004
dbSNP: rs749927570
rs749927570
ANKRD27 ; RGS9BP
1 19 32676628 missense variant C/G;T snv 7.9E-05 0.700 0