Source: GWASCAT ×
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: rs12914385
rs12914385
CHRNA3
8 0.790 0.160 15 78606381 intron variant C/A;T snv 0.800 1.000 1 2010 2017
dbSNP: rs9788721
rs9788721
HYKK
6 1.000 0.040 15 78510527 intron variant C/T snv 0.65 0.800 1.000 1 2010 2017
dbSNP: rs10031466
rs10031466
TRIML2
2 4 188094248 intron variant G/A snv 0.56 0.700 1.000 1 2015 2015
dbSNP: rs1003858
rs1003858
PAPPA
2 9 116202676 intron variant G/C snv 1.1E-02 0.700 1.000 1 2015 2015
dbSNP: rs10041657
rs10041657
FER
2 5 108816727 intron variant G/A snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs1014667
rs1014667
NRXN1
2 2 50521617 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs10195252
rs10195252
COBLL1
6 0.925 0.080 2 164656581 intron variant T/C snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs10245353
rs10245353 		3 7 25818994 intergenic variant C/A snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs10269774
rs10269774
CDK6
2 7 92624658 intron variant G/A snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs10425738
rs10425738
CYP2G1P
2 19 40911822 non coding transcript exon variant G/A snv 0.74 0.700 1.000 1 2016 2016
dbSNP: rs10440708
rs10440708 		2 5 173223484 downstream gene variant A/G snv 4.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs1045241
rs1045241
TNFAIP8
5 1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs10488693
rs10488693
DAGLA
2 11 61717684 intron variant C/T snv 6.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs1049281
rs1049281
HLA-C
2 1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 0.700 1.000 1 2017 2017
dbSNP: rs10501157
rs10501157
TRAF6
2 11 36485319 3 prime UTR variant T/C snv 1.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs10503023
rs10503023 		2 18 59165543 intergenic variant G/A snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs10783615
rs10783615
HOXC12 ; LOC105369775
2 12 53955989 intron variant G/A snv 0.71 0.700 1.000 1 2017 2017
dbSNP: rs10804591
rs10804591 		4 3 129615390 intergenic variant C/A snv 0.63 0.700 1.000 1 2017 2017
dbSNP: rs10842707
rs10842707 		4 12 26318431 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10856789
rs10856789 		2 2 19581401 intergenic variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs10912872
rs10912872 		2 1 171387110 intergenic variant G/T snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs10919388
rs10919388 		4 1 170403362 intergenic variant A/C snv 0.71 0.700 1.000 1 2017 2017
dbSNP: rs10923712
rs10923712
TBX15
4 1 118962811 intron variant G/A snv 0.56 0.700 1.000 1 2017 2017
dbSNP: rs10958852
rs10958852
PTPRD
2 9 10060843 intron variant C/T snv 4.5E-04 0.700 1.000 1 2015 2015
dbSNP: rs10991437
rs10991437
CT70
2 9 104973639 intron variant C/A snv 9.0E-02 0.700 1.000 1 2017 2017