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: rs2074356
rs2074356
HECTD4
12 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 0.800 1.000 2 2011 2017
dbSNP: rs1049296
rs1049296
TF
1 0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 0.800 1.000 1 2011 2011
dbSNP: rs10849915
rs10849915
CCDC63
2 0.925 0.080 12 110895818 intron variant T/C snv 0.39 0.800 1.000 1 2011 2017
dbSNP: rs12229654
rs12229654 		10 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 0.800 1.000 1 2011 2017
dbSNP: rs1229984
rs1229984
ADH1B
6 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.800 1.000 1 2013 2017
dbSNP: rs1534166
rs1534166
SRPRB
1 3 133818223 intron variant A/G snv 0.28 0.800 1.000 1 2011 2011
dbSNP: rs1799899
rs1799899
TF
1 1.000 0.080 3 133756968 missense variant G/A snv 5.2E-02 4.5E-02 0.800 1.000 1 2011 2011
dbSNP: rs1800562
rs1800562
HFE ; LOC108783645
14 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.800 1.000 1 2011 2011
dbSNP: rs2072134
rs2072134
OAS3
1 12 112971371 3 prime UTR variant G/A snv 3.7E-03 0.800 1.000 1 2011 2017
dbSNP: rs2749097
rs2749097 		1 1 63661797 downstream gene variant C/G snv 0.19 0.800 1.000 1 2011 2011
dbSNP: rs3811647
rs3811647
TF
3 0.807 0.120 3 133765185 intron variant G/A snv 0.31 0.800 1.000 1 2011 2011
dbSNP: rs4758317
rs4758317
LMO1 ; LOC105376536
1 11 8229264 intron variant C/A snv 0.57 0.800 1.000 1 2013 2013
dbSNP: rs59677118
rs59677118
NFIB
1 9 14441679 intron variant G/A snv 7.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs671
rs671
ALDH2
10 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.800 1.000 1 2013 2017
dbSNP: rs6943555
rs6943555
AUTS2
1 0.882 0.080 7 70341037 intron variant T/A snv 0.34 0.800 1.000 1 2011 2011
dbSNP: rs10249276
rs10249276 		1 7 118938630 intergenic variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10281955
rs10281955 		1 7 118944637 intergenic variant G/A snv 0.86 0.700 1.000 1 2012 2012
dbSNP: rs10433415
rs10433415 		1 3 133566686 intergenic variant G/T snv 0.57 0.700 1.000 1 2011 2011
dbSNP: rs10935068
rs10935068 		1 3 133543963 upstream gene variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10935070
rs10935070
TOPBP1
1 3 133623144 missense variant T/C;G snv 0.29; 4.0E-06 0.700 1.000 1 2011 2011
dbSNP: rs10935073
rs10935073
TF ; INHCAP
1 3 133720340 intron variant T/C snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs10953881
rs10953881 		1 7 118968071 intergenic variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10953885
rs10953885 		1 7 118968349 intergenic variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs11066015
rs11066015
ACAD10
3 0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 0.700 1.000 1 2013 2013
dbSNP: rs11066280
rs11066280
HECTD4
8 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2013 2013