Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs954767 5 3705936 intergenic variant A/C snv 0.27 2
rs10198275
ADCY3
2 24907673 intron variant A/C snv 0.53 1
rs11681462 2 42125427 intergenic variant A/C snv 0.15 1
rs11931572 4 30084482 intergenic variant A/C snv 1.6E-02 1
rs1215469
LOC105370275
13 80133273 intron variant A/C snv 0.82 1
rs17046596
GPATCH2
1 217549107 intron variant A/C snv 0.22 1
rs1876487
SPR
1.000 0.040 2 72887223 upstream gene variant A/C snv 0.54 1
rs4507125 2 238943036 regulatory region variant A/C snv 0.21 1
rs62380354
LINC01339
5 90189094 intron variant A/C snv 7.4E-02 1
rs7436887 4 155529048 regulatory region variant A/C snv 0.59 1
rs7606205
ARHGAP15
2 143388742 intron variant A/C snv 0.36 1
rs7608483 2 61609100 downstream gene variant A/C snv 0.62 1
rs7989823
COL4A2 ; COL4A1
13 110307296 5 prime UTR variant A/C snv 0.63 1
rs8139817
MICAL3
22 17985603 intron variant A/C snv 0.34 1
rs9348895
LOC105374928
6 11495815 intron variant A/C snv 0.54 1
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 4
rs6418
GML ; CYP11B2
8 142914947 intron variant A/C;G snv 0.42 4
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 3
rs7006531 8 94098516 intron variant A/C;G snv 3
rs12596053
PPL ; LOC105371064
16 4896793 intron variant A/C;G snv 2
rs61879810
PAX6
11 31799919 intron variant A/C;G snv 2
rs903432
PDE10A
6 165761983 intron variant A/C;G snv 2
rs1271309
NCOR2
12 124336159 non coding transcript exon variant A/C;G snv 1
rs1975487
PPP4R3B
2 55581918 intron variant A/C;G snv 1