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: rs174548
rs174548
FADS1 ; FADS2
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 3 2008 2013
dbSNP: rs174455
rs174455
FADS3
5 1.000 0.080 11 61888645 intron variant G/A;C snv 0.700 1.000 2 2012 2013
dbSNP: rs174576
rs174576
FADS2
14 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 2 2012 2013
dbSNP: rs261342
rs261342
LIPC ; ALDH1A2 ; LIPC-AS1
5 15 58438954 intron variant G/A;C;T snv 0.700 1.000 2 2012 2013
dbSNP: rs34121855
rs34121855
MLXIPL
1 7 73626484 upstream gene variant T/C;G snv 0.800 1.000 2 2012 2018
dbSNP: rs3733402
rs3733402
KLKB1
5 1.000 0.040 4 186236880 missense variant G/A;C snv 0.54 0.700 1.000 2 2012 2014
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
29 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 0.700 1.000 2 2012 2013
dbSNP: rs599839
rs599839
PSRC1
27 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 0.700 1.000 2 2011 2012
dbSNP: rs651007
rs651007 		22 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 0.700 1.000 2 2011 2013
dbSNP: rs10057473
rs10057473 		1 5 143507813 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs1007205
rs1007205
DOCK7
1 1 62471241 intron variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1010278
rs1010278 		1 8 57641227 intron variant A/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10120501
rs10120501
PTPRD
1 9 8826767 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10121203
rs10121203
PTPRD
1 9 8833227 intron variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10132646
rs10132646
LOC728755
1 14 27496715 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10144572
rs10144572
LOC728755
1 14 27503663 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10152355
rs10152355
ALDH1A2
1 15 58378979 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10159528
rs10159528
GRID1
1 10 85725660 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs10159927
rs10159927 		1 10 8292500 intergenic variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10168416
rs10168416
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A9
1 2 233688441 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10170033
rs10170033
SLC1A4 ; LINC02245 ; LOC107984063
1 2 64988123 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10171367
rs10171367
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A9
3 2 233689021 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10173355
rs10173355
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A9
6 1.000 2 233688675 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10201247
rs10201247 		1 2 27752104 intergenic variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1023818
rs1023818 		1 13 69152910 intergenic variant A/G;T snv 0.700 1.000 1 2013 2013