Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17883880
CHUK
10 100230590 intron variant T/A snv 1.2E-02 4
rs35782247
FANCD2
3 10048005 missense variant T/G snv 7.0E-03 2.9E-02 2
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs7836284
MSRA
8 10075045 intron variant C/T snv 2.9E-02 2
rs7012397
MSRA
8 10091523 intron variant A/G snv 6.6E-02 2
rs11224571
PGR
11 101047942 intron variant C/A snv 1.2E-02 3
rs10087178
MSRA
8 10111284 intron variant T/C snv 6.6E-02 2
rs7928851
PGR
11 101117160 intron variant C/A snv 1.7E-02 3
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs10107815
MSRA
8 10156645 intron variant G/C snv 5.1E-02 4
rs7952037 11 102379653 downstream gene variant C/T snv 1.9E-02 3
rs7001567
MSRA
8 10257027 intron variant C/G snv 3.7E-02 4
rs5030339
LOC105372272 ; ICAM1
19 10269461 intron variant G/A snv 3.4E-03 5
rs5030359
ICAM1
19 10277786 intron variant G/A snv 2.1E-03 3
rs5030361
ICAM1
19 10278833 intron variant C/T snv 6.8E-04 4
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs3212121
XRCC3 ; KLC1
14 103698185 3 prime UTR variant T/C snv 1.9E-02 2
rs10271556
NAMPT
7 106258428 intron variant C/T snv 5.6E-02 4
rs11193085
SORCS1
10 106873848 intron variant G/A snv 8.8E-02 3
rs13465
ILF3
19 10692116 3 prime UTR variant A/C;G snv 3
rs11813704
SORCS1
10 107102114 intron variant G/T snv 3.1E-02 2
rs3218688
ATM
11 108268595 missense variant C/T snv 3.2E-05 2.1E-05 4
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs10858082
CELSR2
1 109256099 intron variant G/A snv 0.48 3