Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11779535 8 100376055 downstream gene variant G/A;C;T snv 1
rs7939778 11 100636316 intergenic variant G/A;C snv 1
rs76382185 1 101182070 regulatory region variant C/T snv 8.0E-02 1
rs146490475
S1PR1 ; LOC101928370
1 101236803 upstream gene variant T/C snv 1.9E-02 1
rs3835397
LOC101928370 ; S1PR1
1 101236992 splice donor variant G/- del 9.2E-02 1
rs41287280
S1PR1
1 101239021 missense variant C/A;G;T snv 4.0E-06; 1.4E-02 1
rs77372977 1 101267901 downstream gene variant C/G;T snv 1
rs77046277 1 101279090 intergenic variant C/G snv 1.2E-03 1
rs17041439
SPIC
12 101479462 intron variant A/C snv 7.0E-02 2
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs5026472
MANBA
4 102633616 intron variant C/A;G snv 1
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs2224234 14 102915701 downstream gene variant A/C snv 0.33 1
rs35251378 19 10349293 downstream gene variant G/A snv 0.24 1
rs10022109
TET2
4 105166665 intron variant A/G snv 0.20 1
rs546941547
TET2-AS1 ; TET2
4 105204229 intron variant TATA/-;TA;TATATA delins 6.5E-02 1
rs6568490
SCML4
6 107732765 intron variant G/T snv 0.20 1
rs36084354
ARHGAP45
19 1079960 missense variant G/A snv 5.7E-02 5.9E-02 3
rs11250079
PINX1
8 10815498 intron variant T/C snv 0.30 1
rs117706999
EXPH5
11 108536216 intron variant G/A snv 1.5E-02 1
rs17229044
CLEC16A
1.000 0.120 16 10969079 intron variant C/T snv 0.16 1
rs518785 1 110817180 regulatory region variant G/A snv 0.82 1
rs7576541
ACOXL
2 110849824 intron variant C/A;G;T snv 1
rs150784178
MIR4435-2HG ; ACOXL-AS1 ; ACOXL
2 111116484 intron variant CTCTGAAAACCTGAAATG/- delins 0.11 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61