Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 1
rs12822507
CREBL2
1.000 0.080 12 12620587 intron variant A/G snv 0.32 1
rs131654
UBE2L3
1.000 0.080 22 21562901 intron variant G/A;T snv 1
rs13194781
H2BC15
1.000 0.080 6 27847861 intron variant A/G snv 5.3E-02 1
rs13195509
BTN2A1
1.000 0.080 6 26463432 missense variant G/A snv 5.7E-02 6.4E-02 1
rs13205210
UHRF1BP1
1.000 0.080 6 34864079 missense variant T/C snv 0.11 0.13 1
rs13239597
TNPO3 ; TPI1P2
0.882 0.080 7 129055929 non coding transcript exon variant C/A snv 9.0E-02 1
rs1385374
SLC15A4
1.000 0.080 12 128816149 intron variant C/T snv 9.1E-02 1
rs1419183
ZSCAN26
1.000 0.080 6 28275017 intron variant A/C snv 0.17 1
rs1535001
ANKS1A
0.925 0.080 6 34959503 intron variant A/G snv 0.47 1
rs16833239
STAT4
1.000 0.080 2 191075534 intron variant G/A snv 8.0E-02 1
rs200953
H1-5
1.000 0.080 6 27869489 upstream gene variant T/C snv 0.12 1
rs200991
H2BC15
1.000 0.080 6 27847716 intron variant C/A snv 0.21 1
rs200997
H2BC15
1.000 0.080 6 27844037 intron variant G/A snv 0.41 1
rs2022013
NMNAT2
1.000 0.080 1 183384718 intron variant C/T snv 0.51 1
rs205284 1.000 0.080 6 34584135 downstream gene variant C/G;T snv 1
rs2066807
STAT2
0.925 0.080 12 56346898 missense variant C/G snv 4.9E-02 4.6E-02 1
rs2071725
SCUBE1 ; LOC105373051
1.000 0.080 22 43213754 intron variant G/A snv 0.14 1
rs2084654 1.000 0.080 7 129089074 intergenic variant A/G snv 0.39 1
rs2176082
PXK
0.925 0.080 3 58345459 intron variant G/A snv 0.36 1
rs2275247
KIAA0319L
0.925 0.080 1 35442850 intron variant T/C snv 0.26 1
rs2303745
ABHD8 ; DDA1
1.000 0.080 19 17309480 intron variant G/C;T snv 1
rs2667978
LYN
1.000 0.080 8 55985392 intron variant A/G snv 0.18 1
rs2785197
LOC105376626
1.000 0.080 11 35071523 intergenic variant A/G;T snv 1
rs3129975 1.000 0.080 6 30764277 intron variant T/C;G snv 1