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: rs272889
rs272889
SLC22A4 ; MIR3936HG
2 5 132329685 intron variant A/G snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs4149081
rs4149081
SLCO1B1
5 1.000 0.040 12 21225087 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs4253252
rs4253252
KLKB1
3 4 186236304 intron variant T/G snv 0.56 0.700 1.000 1 2011 2011
dbSNP: rs4329
rs4329
ACE
2 17 63486097 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs4481233
rs4481233
SLC2A9
5 0.925 0.120 4 9954455 intron variant C/T snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs477992
rs477992
PHGDH
4 1 119714953 intron variant A/G snv 0.69 0.700 1.000 1 2011 2011
dbSNP: rs494562
rs494562 		2 6 85407411 intergenic variant A/G snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs503279
rs503279
FUT2 ; LOC105447645
2 19 48705753 3 prime UTR variant T/C snv 0.48 0.700 1.000 1 2011 2011
dbSNP: rs603424
rs603424
PKD2L1
13 1.000 0.080 10 100315722 intron variant G/A snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs612169
rs612169
ABO
10 9 133268030 intron variant G/A snv 0.700 1.000 1 2011 2011
dbSNP: rs6499165
rs6499165
SLC7A6 ; SLC7A6OS
2 16 68292297 non coding transcript exon variant A/C snv 0.80 0.700 1.000 1 2011 2011
dbSNP: rs6558295
rs6558295
GPAA1
2 8 144084619 intron variant C/G snv 8.1E-02 0.14 0.700 1.000 1 2011 2011
dbSNP: rs662138
rs662138
SLC22A1
2 6 160143444 intron variant C/G snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs7094971
rs7094971
SLC16A9
4 0.925 0.120 10 59689806 intron variant A/G snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs7200543
rs7200543
PDXDC1
6 16 15036113 synonymous variant A/G snv 0.35 0.30 0.700 1.000 1 2011 2011
dbSNP: rs7760535
rs7760535
REV3L ; MFSD4B
3 6 111425880 intron variant G/C snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs8396
rs8396
ETFDH ; PPID
4 4 158709665 3 prime UTR variant T/C snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs887829
rs887829
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A1 ; UGT1A3
18 0.763 0.280 2 233759924 intron variant C/T snv 0.36 0.700 1.000 1 2011 2011
dbSNP: rs9332998
rs9332998
CYP4A11
2 1 46938514 intron variant T/C snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs9393903
rs9393903
ELOVL2 ; ELOVL2-AS1
3 6 11042676 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs174547
rs174547
FADS1 ; FADS2
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.800 1.000 2 2011 2016
dbSNP: rs10401969
rs10401969
SUGP1
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.700 1.000 1 2016 2016
dbSNP: rs12310617
rs12310617 		16 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs12369179
rs12369179
ZCCHC8
16 0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs12420422
rs12420422 		16 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 0.700 1.000 1 2016 2016