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: rs10900585
rs10900585
ATP2B4
1 1.000 0.040 1 203684896 intron variant G/T snv 0.81 0.810 1.000 1 2012 2013
dbSNP: rs334
rs334
HBB
19 0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 0.810 1.000 1 2009 2018
dbSNP: rs11036238
rs11036238 		1 1.000 0.040 11 5204405 upstream gene variant G/C snv 0.21 0.800 1.000 1 2009 2009
dbSNP: rs12788102
rs12788102
MMP26 ; OR51F1
1 1.000 0.040 11 4769345 synonymous variant A/G snv 9.5E-02 9.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs1469170
rs1469170 		1 1.000 0.040 11 110870290 intergenic variant A/G snv 0.55 0.800 1.000 1 2013 2013
dbSNP: rs372091
rs372091
HBE1 ; HBG2 ; OR51B5
1 1.000 0.040 11 5496926 intron variant A/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs6503319
rs6503319
MYH3
1 1.000 0.040 17 10670842 downstream gene variant C/T snv 0.31 0.800 1.000 1 2009 2009
dbSNP: rs6755404
rs6755404
ZNF804A
1 1.000 0.040 2 184932501 intron variant A/C snv 0.82 0.800 1.000 1 2013 2013
dbSNP: rs8176719
rs8176719
ABO
4 0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35 0.800 1.000 1 2012 2012
dbSNP: rs8176722
rs8176722
ABO
1 1.000 0.040 9 133257367 intron variant C/A snv 0.13 0.12 0.800 1.000 1 2013 2013
dbSNP: rs9940464
rs9940464
CDH13
1 1.000 0.040 16 83327170 intron variant T/C snv 0.39 0.800 1.000 1 2013 2013
dbSNP: rs11335470
rs11335470
LINC00944
1 1.000 0.040 12 126753075 intron variant T/- delins 0.94 0.700 1.000 1 2018 2018
dbSNP: rs113449872
rs113449872 		1 1.000 0.040 5 43909241 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs114169033
rs114169033
FRG1-DT
1 1.000 0.040 4 189796550 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs144312179
rs144312179
FAM155A
1 1.000 0.040 13 107575665 intron variant A/G snv 7.4E-03 0.700 1.000 1 2018 2018
dbSNP: rs149085856
rs149085856 		1 1.000 0.040 17 12496210 intergenic variant C/-;CC;CCC delins 0.700 1.000 1 2018 2018
dbSNP: rs17624383
rs17624383 		1 1.000 0.040 7 53609144 intergenic variant G/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs186873296
rs186873296 		1 1.000 0.040 4 143781321 intron variant A/G snv 2.5E-03 0.700 1.000 1 2015 2015
dbSNP: rs1878468
rs1878468
TENM3 ; TENM3-AS1
1 1.000 0.040 4 181901179 intron variant G/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs2967790
rs2967790
KLHL3
1 1.000 0.040 5 137676072 intron variant C/T snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs3133394
rs3133394
LOC105369574
1 1.000 0.040 11 130547627 upstream gene variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs6588252
rs6588252 		1 1.000 0.040 1 67273345 upstream gene variant G/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs6682413
rs6682413 		1 1.000 0.040 1 67265931 downstream gene variant G/A snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs73505850
rs73505850
CSMD1
1 1.000 0.040 8 4897316 intron variant G/A snv 2.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs73832816
rs73832816 		1 1.000 0.040 4 99508600 upstream gene variant G/A snv 1.2E-02 0.700 1.000 1 2018 2018