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: rs4846914
rs4846914
GALNT2
6 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.700 1.000 5 2008 2013
dbSNP: rs1689800
rs1689800
LINC01344
2 1 182199750 intron variant A/G snv 0.34 0.700 1.000 2 2010 2013
dbSNP: rs2144300
rs2144300
GALNT2
7 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.700 1.000 2 2008 2012
dbSNP: rs4660293
rs4660293
PABPC4
5 1 39562508 non coding transcript exon variant A/C;G snv 0.700 1.000 2 2010 2013
dbSNP: rs4846918
rs4846918
GALNT2
3 1 230164840 intron variant C/G;T snv 0.700 1.000 2 2012 2012
dbSNP: rs599839
rs599839
PSRC1
27 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 0.700 1.000 2 2012 2013
dbSNP: rs10305650
rs10305650
ARNT
2 1 150876501 intron variant G/A;C snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs10305685
rs10305685
ARNT
2 1 150838529 intron variant T/C snv 5.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs10489615
rs10489615
GALNT2
3 1 230169242 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs11568026
rs11568026
AGT
2 1 230711777 intron variant A/G snv 3.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs11571111
rs11571111
REN
4 1 204161105 intron variant C/A snv 5.0E-03 0.700 1.000 1 2012 2012
dbSNP: rs11804107
rs11804107
SLC16A1
2 1 112929525 intron variant C/A snv 1.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs12089132
rs12089132
IL6R ; IL6R-AS1
2 1 154405860 intron variant T/C snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs12092977
rs12092977
FAF1 ; LOC112268262
2 1 50944845 intron variant T/C snv 2.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs12097137
rs12097137 		3 1 101243889 downstream gene variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12145743
rs12145743
RRNAD1
4 1 156730859 intron variant T/G snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs12740374
rs12740374
CELSR2
16 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.700 1.000 1 2012 2012
dbSNP: rs12748152
rs12748152 		8 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs1321655
rs1321655
ATP1A2
5 1 160124668 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1456649
rs1456649
FMN2
5 1 240288305 intron variant G/C snv 3.0E-03 0.700 1.000 1 2012 2012
dbSNP: rs1510291
rs1510291
NOS1AP
2 1 162358271 intron variant C/T snv 3.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs1552481
rs1552481
IL6R ; IL6R-AS1
2 1 154403877 non coding transcript exon variant C/T snv 0.94 0.700 1.000 1 2012 2012
dbSNP: rs17131304
rs17131304
CTH
2 1 70427232 intron variant A/T snv 3.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs17315646
rs17315646
GALNT2
4 1 230159560 intron variant C/A;G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs1912439
rs1912439
NOS1AP
2 1 162324355 intron variant A/G snv 0.98 0.700 1.000 1 2012 2012