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: rs41278532
rs41278532
STOX1
1 1.000 0.040 10 68886270 missense variant A/T snv 2.7E-03 2.4E-03 0.700 1.000 1 2005 2005
dbSNP: rs556362193
rs556362193
STOX1
1 1.000 0.040 10 68827676 missense variant G/C;T snv 1.0E-02 0.700 1.000 1 2005 2005
dbSNP: rs10509305
rs10509305
STOX1
1 1.000 0.040 10 68885620 missense variant A/C;T snv 0.22; 4.0E-06 0.700 0
dbSNP: rs1341667
rs1341667
STOX1
4 0.925 0.040 10 68882104 missense variant T/C snv 0.62 0.57 0.700 0