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: rs2108622
rs2108622
CYP4F2
20 0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 0.700 1.000 1 2014 2014
dbSNP: rs2387326
rs2387326 		2 10 128135192 intergenic variant C/T snv 0.24 0.700 1.000 1 2007 2007
dbSNP: rs4645543
rs4645543 		1 8 139483999 intergenic variant C/T snv 4.6E-02 0.700 1.000 1 2014 2014
dbSNP: rs4852146
rs4852146
CTNNA2
1 2 79397862 intron variant C/T snv 0.71 0.700 1.000 1 2014 2014
dbSNP: rs6862909
rs6862909 		1 5 115784737 intergenic variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs964184
rs964184
ZPR1
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.700 1.000 1 2014 2014