Source: GWASDB ×
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: rs10174949
rs10174949
LINC00299
1 1.000 0.080 2 8302118 non coding transcript exon variant G/A snv 0.23 0.800 1.000 1 2013 2018
dbSNP: rs10189629
rs10189629 		2 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 0.800 1.000 1 2013 2013
dbSNP: rs10497813
rs10497813
PLCL1
1 2 198049348 intron variant G/T snv 0.43 0.800 1.000 1 2013 2013
dbSNP: rs1064213
rs1064213
PLCL1
1 2 198085516 missense variant G/A snv 0.44 0.41 0.800 1.000 1 2013 2017
dbSNP: rs10893845
rs10893845 		1 11 128316987 regulatory region variant T/G snv 0.36 0.800 1.000 1 2013 2013
dbSNP: rs12339348
rs12339348
IL33 ; LOC107987046
1 1.000 0.080 9 6233082 intron variant A/G;T snv 0.800 1.000 1 2013 2018
dbSNP: rs1438673
rs1438673 		1 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 0.800 1.000 1 2013 2018
dbSNP: rs17228058
rs17228058
SMAD3
1 1.000 0.040 15 67157967 intron variant A/G snv 0.17 0.800 1.000 1 2013 2013
dbSNP: rs17294280
rs17294280
SMAD3
1 0.882 0.120 15 67175947 intron variant A/G snv 0.19 0.800 1.000 1 2013 2016
dbSNP: rs17388568
rs17388568
ADAD1
3 0.827 0.280 4 122408207 intron variant G/A snv 0.20 0.800 1.000 1 2013 2013
dbSNP: rs1775550
rs1775550 		1 10 9010779 regulatory region variant G/A;C snv 0.800 1.000 1 2013 2016
dbSNP: rs1837253
rs1837253 		2 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 0.800 1.000 1 2013 2018
dbSNP: rs1998359
rs1998359
TTC6
1 14 37607943 intron variant C/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs20541
rs20541
IL13 ; TH2LCRR
5 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 0.800 1.000 1 2013 2013
dbSNP: rs2056417
rs2056417
PEX14
1 1 10521601 intron variant G/A snv 0.25 0.800 1.000 1 2013 2013
dbSNP: rs2101521
rs2101521
TLR1
1 0.925 0.080 4 38809930 intron variant G/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs2107357
rs2107357 		1 16 27399508 upstream gene variant A/G snv 0.85 0.800 1.000 1 2013 2013
dbSNP: rs2155219
rs2155219 		7 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 0.800 1.000 1 2013 2013
dbSNP: rs367023
rs367023
LINC00299
1 1.000 0.040 2 8309993 intron variant A/G snv 0.35 0.800 1.000 1 2013 2016
dbSNP: rs4795400
rs4795400
GSDMB
3 0.925 0.080 17 39910767 intron variant C/T snv 0.36 0.800 1.000 1 2013 2016
dbSNP: rs6021270
rs6021270
NFATC2
1 20 51524725 intron variant T/C snv 5.7E-02 0.800 1.000 1 2013 2013
dbSNP: rs6457730
rs6457730
LOC107986537
1 6 33518955 intergenic variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs6473223
rs6473223 		1 8 80355920 intron variant T/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs6594499
rs6594499 		1 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 0.800 1.000 1 2013 2017
dbSNP: rs6906021
rs6906021
HLA-DQB1-AS1
3 0.827 0.320 6 32658534 upstream gene variant T/C snv 0.47 0.800 1.000 1 2013 2013