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: rs10989692
rs10989692 		1 9 101912273 intergenic variant G/A snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs1934951
rs1934951
CYP2C8
4 0.925 0.160 10 95038791 intron variant C/T snv 0.24 0.700 1.000 1 2008 2008
dbSNP: rs2154490
rs2154490
BACH1 ; GRIK1
1 21 29543641 intron variant A/G snv 0.75 0.700 1.000 1 2015 2015
dbSNP: rs2229288
rs2229288
ZFHX3 ; LOC101927978
1 16 72794405 missense variant C/A snv 2.5E-03 2.1E-03 0.700 1.000 1 2015 2015
dbSNP: rs7925908
rs7925908 		1 11 131276855 intron variant T/C snv 0.64 0.700 1.000 1 2015 2015