Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs11229
PRRC2A
0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
rs3117583
APOM ; BAG6
0.925 0.200 6 31651799 5 prime UTR variant A/G snv 0.14 0.17 3
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 2
rs4678
VARS2
0.925 0.200 6 30926164 missense variant G/A snv 0.14 0.15 2
rs2517598
TRIM31 ; TRIM31-AS1
0.851 0.280 6 30112497 synonymous variant G/A snv 0.14 0.13 4
rs2071481
TAP1 ; PSMB9
1.000 0.120 6 32852088 intron variant T/C snv 0.14 0.11 1
rs3134940
AGER
0.925 0.200 6 32182039 intron variant T/C snv 0.13 0.14 2
rs492899
CYP21A2 ; SKIV2L
0.882 0.240 6 31965741 intron variant T/C snv 0.12 0.15 2
rs2523989
TRIM31 ; TRIM31-AS1
0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 4
rs3094073
HLA-L ; HCG17
0.882 0.240 6 30263447 non coding transcript exon variant G/A snv 0.12 0.12 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 1
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 1
rs3134942
NOTCH4
0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 6
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 6
rs9267532
LY6G5B ; CSNK2B
1.000 0.120 6 31672202 missense variant C/T snv 7.4E-02 7.9E-02 2
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
rs7750641
TCF19
0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 5
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs2071554
HLA-DOB
0.925 0.200 6 32816899 missense variant C/A;T snv 4.1E-06; 6.2E-02 2
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs9262143
PPP1R18
0.851 0.240 6 30685004 missense variant C/G;T snv 4.1E-06; 6.1E-02 4
rs7775397
TSBP1-AS1 ; TSBP1
0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 6
rs1150752
TNXB
0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02 3
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11