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: rs111325002
rs111325002 		2 1.000 0.080 3 96134788 intergenic variant A/G snv 8.6E-03 0.700 1.000 1 2014 2014
dbSNP: rs150954431
rs150954431
NCOR2
2 1.000 0.080 12 124517777 intron variant C/T snv 1.6E-02 0.700 1.000 1 2014 2014
dbSNP: rs2005290
rs2005290
OR3A2
2 1.000 0.080 17 3284718 intron variant C/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs2629540
rs2629540
FAM53B
4 0.925 0.080 10 124737579 intron variant G/C snv 0.18 0.700 1.000 1 2014 2014