Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13262595
LOC107986983 ; TSNARE1
1.000 0.040 8 142235609 intron variant A/C;G snv 3
rs6119267
NOL4L-DT ; NOL4L
20 32576112 intron variant C/A;G snv 3
rs76076331
PDIA6
1.000 0.040 2 10837459 intron variant C/T snv 1.0E-01 3
rs11545169
PSMD2
3 184302754 missense variant G/T snv 0.13 0.11 3
rs11765189
PTPRN2
1.000 0.040 7 157743285 intron variant A/G snv 0.25 3
rs1131017
RPS26 ; LOC105369780
0.925 0.160 12 56042145 5 prime UTR variant C/A;G;T snv 8.0E-06; 8.0E-06; 0.62; 1.1E-04 3
rs75757892
RREB1
6 7232156 intron variant C/T snv 0.12 3
rs9616914
SHANK3
1.000 0.040 22 50678709 intron variant G/A snv 0.35 0.36 3
rs7963801
SYT1
12 79291446 intron variant T/C snv 0.70 3
rs613872
TCF4
0.851 0.120 18 55543071 intron variant G/T snv 0.88 3
rs62154720
TGFBRAP1
1.000 0.040 2 105306623 intron variant C/T snv 9.2E-02 3
rs6870983
TMEM161B-AS1
5 88401716 intron variant C/T snv 0.29 3
rs4396807
TRIOBP
22 37742372 intron variant G/C snv 0.38 3
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10789285 1.000 0.040 1 69322799 intergenic variant T/G snv 0.33 2
rs10922907 1 90727492 downstream gene variant A/G;T snv 2
rs1107960 14 54917622 intergenic variant T/A snv 0.42 2
rs11793831 9 23362313 intron variant G/A;T snv 2
rs12028010 1 41298799 intron variant T/C snv 0.19 2
rs13259607 8 70439812 intergenic variant C/T snv 0.15 2
rs1343775 1 41292321 intron variant A/G snv 0.17 2
rs142601917 12 120914271 upstream gene variant C/A;G;T snv 2
rs1473634 8 21057805 intron variant A/G snv 0.22 2
rs1492014 3 94352637 intergenic variant T/C;G snv 2