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: rs2080304
rs2080304
FLACC1
1 2 201321699 intron variant G/C snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs2110690
rs2110690
FLACC1
1 2 201320409 intron variant A/G snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs2349073
rs2349073
FLACC1
1 2 201322263 intron variant C/A snv 0.75 0.700 1.000 1 2012 2012
dbSNP: rs2378002
rs2378002 		1 1 218749016 intergenic variant G/T snv 5.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs2409764
rs2409764
FAM167A ; FAM167A-AS1
1 8 11423764 3 prime UTR variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs26704
rs26704
PDE4D
1 5 59237827 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2803270
rs2803270
AGBL4
1 1 48565566 intron variant C/T snv 0.61 0.700 1.000 1 2012 2012
dbSNP: rs2984526
rs2984526 		1 9 72372344 intergenic variant C/G snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs3398
rs3398
ZFAND5 ; LINC01504
1 9 72354160 3 prime UTR variant G/A snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs3807390
rs3807390
AMPH
1 7 38533831 intron variant T/C snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs4148641
rs4148641
ABCC8
1 11 17399926 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs4283388
rs4283388 		1 2 172374994 downstream gene variant C/T snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs4503732
rs4503732 		1 15 46350065 intron variant C/A;G;T snv 0.92 0.700 1.000 1 2012 2012
dbSNP: rs4788074
rs4788074
SGF29
1 16 28582276 intron variant G/A snv 0.32 0.700 1.000 1 2012 2012
dbSNP: rs4851005
rs4851005
IL18R1
2 2 102395092 intron variant C/T snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs4872018
rs4872018
PEBP4
1 8 22794657 intron variant G/T snv 0.60 0.700 1.000 1 2012 2012
dbSNP: rs4908343
rs4908343
AHDC1
1 1 27605187 upstream gene variant G/A snv 0.61 0.700 1.000 1 2010 2010
dbSNP: rs4970821
rs4970821
SLC25A24P1
1 1 108316692 intron variant T/C snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs5753220
rs5753220
PES1
1 22 30590363 intron variant T/C snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs581037
rs581037
AHR
1 7 17050319 intron variant C/T snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs5996074
rs5996074
SREBF2
3 22 41840333 intron variant G/A snv 0.74 0.700 1.000 1 2012 2012
dbSNP: rs6023640
rs6023640 		1 20 54842266 intergenic variant T/G snv 0.73 0.700 1.000 1 2010 2010
dbSNP: rs6140125
rs6140125
SLC52A3
1 20 764903 intron variant C/A snv 1.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs6435079
rs6435079
FLACC1
1 2 201335608 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs6714736
rs6714736
FLACC1
1 2 201349425 intron variant C/T snv 0.63 0.700 1.000 1 2012 2012