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: rs2835872
rs2835872
KCNJ6
3 1.000 0.080 21 37654970 intron variant G/A snv 0.26 0.800 1.000 1 2012 2012
dbSNP: rs1229984
rs1229984
ADH1B
25 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.700 1.000 4 2013 2019
dbSNP: rs1000579
rs1000579
STX18-AS1
3 1.000 0.080 4 4717767 intron variant A/G snv 0.44 0.700 1.000 2 2012 2017
dbSNP: rs1789891
rs1789891
ADH1B
3 1.000 0.080 4 99329262 intron variant C/A snv 0.13 0.700 1.000 2 2012 2017
dbSNP: rs2066702
rs2066702
ADH1B
3 0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 0.700 1.000 2 2014 2019
dbSNP: rs10196867
rs10196867
CTNNA2
5 0.925 0.080 2 79751234 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10198241
rs10198241 		4 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs10211296
rs10211296
CSRNP3
3 1.000 0.080 2 165633833 intron variant A/G snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs10392
rs10392
PPP1R16B
6 0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs11066001
rs11066001
BRAP
3 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs11075992
rs11075992
FTO
3 1.000 0.080 16 53786154 intron variant T/C snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs115357105
rs115357105 		4 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs1154433
rs1154433
ADH1B
3 1.000 0.080 4 99332551 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115460205
rs115460205
FSTL5
3 1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs11681792
rs11681792
NRXN1
4 1.000 0.080 2 49957256 intron variant C/T snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs11825659
rs11825659
IGSF9B
4 0.925 0.080 11 133925624 intron variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12180309
rs12180309 		4 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs12544026
rs12544026
NCALD
4 0.925 0.080 8 101819970 intron variant G/A snv 0.85 0.700 1.000 1 2017 2017
dbSNP: rs1260326
rs1260326
GCKR
55 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2019 2019
dbSNP: rs12639833
rs12639833
ADH1B ; ADH1C
3 1.000 0.080 4 99346215 intron variant C/T snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs12898370
rs12898370
HMG20A
3 1.000 0.080 15 77516256 intergenic variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs13107325
rs13107325
SLC39A8
24 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs1316543
rs1316543
GRK5
3 1.000 0.080 10 119445148 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs139438618
rs139438618
SEMA3A
4 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs141424017
rs141424017 		3 1.000 0.080 7 115311376 intergenic variant -/CAA ins 0.700 1.000 1 2019 2019