Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3771608
PKP4
2 158563227 intron variant A/C snv 0.46 1
rs3856395
KIF3C
2 25936094 intron variant A/C snv 0.39 1
rs463312
TUBB1
1.000 0.040 20 59022915 missense variant A/C snv 7.7E-02 5.7E-02 1
rs4803446
AXL
19 41220262 intron variant A/C snv 0.35 1
rs627804 15 65441702 downstream gene variant A/C snv 0.57 1
rs6540549 1 209749323 downstream gene variant A/C snv 0.42 1
rs6673347
DEGS1
1 224179934 intron variant A/C snv 0.25 1
rs724055 22 30279934 upstream gene variant A/C snv 0.59 1
rs730126 2 12751350 intergenic variant A/C snv 0.40 1
rs7828
JAG1
20 10638366 3 prime UTR variant A/C snv 0.27 1
rs7938033
PICALM
11 85991087 intron variant A/C snv 0.40 1
rs9427403
HSPA6 ; FCGR2A
1 161524532 intron variant A/C snv 0.15 1
rs9484829
ZC2HC1B
6 143924474 intron variant A/C snv 0.10 1
rs9521025
MYO16
13 108769778 intron variant A/C snv 0.32 1
rs9861443
CGGBP1
3 88147061 intron variant A/C snv 0.57 1
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs1997595 21 15205839 intron variant A/C;G snv 3
rs573455
CEP164
11 117397168 missense variant A/C;G snv 0.47 2
rs7187776
TUFM ; SH2B1
16 28846324 5 prime UTR variant A/C;G snv 2
rs7520050
MAST2
1 45966433 intron variant A/C;G snv 2
rs11638511
LOC105370911
15 78259585 intron variant A/C;G snv 1
rs116990752
LINC00271
6 135589773 intron variant A/C;G snv 9.3E-03 1
rs12524651
TAF8
6 42087094 3 prime UTR variant A/C;G snv 1