Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10941191 1.000 0.040 5 34504693 intergenic variant C/A;T snv 3
rs11123169
PSD4
1.000 0.080 2 113209498 upstream gene variant C/A;T snv 3
rs12428035 13 95648618 upstream gene variant C/A;T snv 3
rs143193096
IGF1R
15 98916098 missense variant G/A;C snv 8.4E-05; 4.0E-06 3
rs148240484
DPEP1
1.000 0.080 16 89637333 missense variant G/A;C;T snv 5.3E-04; 3.9E-04; 4.0E-06 3
rs16942751
AQP4-AS1
1.000 0.080 18 26813249 intron variant C/A;T snv 3
rs227731 0.882 0.120 17 56695877 intergenic variant T/A;G snv 3
rs2279463
SLC22A2
1.000 0.080 6 160247357 intron variant A/G;T snv 3
rs2421556
TPRKB
1.000 0.040 2 73733254 intron variant G/C;T snv 3
rs2467853
SPATA5L1
1.000 0.080 15 45406595 intron variant T/A;G snv 3
rs2542713
DAB2 ; C9
1.000 0.040 5 39385539 intron variant A/C;G snv 3
rs2923008
HLA-B
1.000 0.040 6 31349134 intron variant G/A;T snv 3
rs3812035
SLC34A1
1.000 0.040 5 177390142 3 prime UTR variant G/A;T snv 3
rs413988
TPPP
1.000 0.040 5 698535 intergenic variant C/G;T snv 3
rs4690095
RGS12
4 3419582 intron variant C/G;T snv 3
rs4744712
PIP5K1B
1.000 0.080 9 68819791 intron variant A/C;T snv 3
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 3
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 3
rs60307791 1.000 0.040 11 65767714 intron variant TT/-;T;TTT;TTTT delins 3
rs6145546
GATM
1.000 0.040 15 45376406 intron variant CTCTTCAGGAAG/-;CTCTTCAGGAAGCTCTTCAGGAAG delins 3
rs7012637 8 9315699 intron variant G/A;C snv 3
rs7024579
QSOX2
9 136208567 3 prime UTR variant C/A;T snv 3
rs7252778
SLC7A9
1.000 0.080 19 32869463 intron variant C/A;T snv 3
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 3
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05 2