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: rs10517480
rs10517480 		2 4 59883111 intergenic variant A/T snv 0.27 0.700 1.000 1 2008 2008
dbSNP: rs174548
rs174548
FADS1 ; FADS2
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs4453795
rs4453795
FGF12
2 3 192376186 intron variant A/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs4775041
rs4775041
ALDH1A2
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 1 2008 2008
dbSNP: rs9924951
rs9924951
RBFOX1
2 16 7454852 intron variant G/A snv 0.39 0.700 1.000 1 2008 2008
dbSNP: rs1000778
rs1000778
FADS3
3 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs1007323
rs1007323
SYCP2L ; LOC101928191
1 6 10953011 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10220265
rs10220265 		1 13 103397233 downstream gene variant G/A snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs10498676
rs10498676
ELOVL2
3 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs1058694
rs1058694
AGPAT3
1 21 43984239 3 prime UTR variant C/T snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs10792320
rs10792320 		1 11 61978819 intergenic variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs108499
rs108499
MYRF ; TMEM258
2 11 61779765 intron variant C/T snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs10897208
rs10897208 		1 11 62024415 intergenic variant A/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs1109748
rs1109748
BEST1 ; LOC107984334
2 11 61955173 synonymous variant C/A snv 0.21 0.11 0.700 1.000 1 2011 2011
dbSNP: rs11230815
rs11230815 		2 11 61868654 downstream gene variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11230874
rs11230874 		1 11 62028114 intergenic variant T/G snv 6.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs1145652
rs1145652 		1 5 165337081 intergenic variant A/G snv 9.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs11730235
rs11730235
STIM2
1 4 26922822 intron variant G/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs12190237
rs12190237
SYCP2L
1 6 10922405 intron variant G/A snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs12195587
rs12195587
ELOVL2
1 6 10989709 synonymous variant G/A snv 0.12 0.11 0.700 1.000 1 2011 2011
dbSNP: rs12199131
rs12199131
SYCP2L ; LOC101928191
1 6 10932336 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12200867
rs12200867
SYCP2L ; LOC101928191
1 6 10939591 intron variant C/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs12207488
rs12207488
SYCP2L ; LOC101928191
1 6 10952103 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12213249
rs12213249
SYCP2L
1 6 10926709 intron variant C/T snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs12214825
rs12214825
SYCP2L ; LOC101928191
1 6 10933145 intron variant C/T snv 0.20 0.700 1.000 1 2011 2011