Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3818666
MOK
14 102304810 intron variant C/T snv 4.5E-02 1
rs7827839
UBR5
8 102341502 intron variant C/T snv 0.59 1
rs141936164
LOC105377621
4 102480566 intergenic variant A/G snv 0.27 1
rs1998422
LOC105370679
14 102514656 upstream gene variant G/A;C snv 1
rs4900538
LOC105370680
14 102527728 intergenic variant T/A;C;G snv 2
rs139247810
WBP1L
10 102801321 intron variant T/G snv 3.0E-03 1
rs12783467
CNNM2
10 102948555 intron variant A/G snv 0.21 1
rs200510190
CNNM2
10 103031838 intron variant C/- del 0.41 2
rs1046411
CNNM2
10 103078059 3 prime UTR variant G/A snv 0.32 1
rs9324058
EXOC3L4
14 103104598 non coding transcript exon variant A/G snv 0.47 1
rs2288789
MACIR
5 103264823 intron variant G/A snv 0.31 2
rs17616316 14 103356425 regulatory region variant C/G snv 7.6E-02 1
rs77697190 14 103380462 upstream gene variant C/T snv 7.9E-02 1
rs75577686
SH3PXD2A
10 103619372 intron variant T/G snv 2.6E-02 1
rs10786774
STN1
10 103884565 intron variant G/C snv 0.90 1
rs7916093
LOC102724351
10 103958628 intergenic variant T/C snv 0.16 2
rs1576368
LOC105376193
9 103987509 intergenic variant A/G snv 0.24 1
rs10772280
KLRC2
12 10428441 intron variant C/A;T snv 2
rs62329718 4 104836902 intron variant T/A snv 2.6E-02 1
rs113549824 4 105030032 intron variant C/A snv 3.6E-02 1
rs3825762
BRF1
14 105286067 intron variant T/C snv 0.30 1
rs72954323
PPA2
4 105466947 intron variant G/A snv 8.0E-02 1
rs892080
CDKN2D
19 10570058 upstream gene variant G/C;T snv 1
rs1104888
LOC107986755 ; C7orf50
7 1066376 intron variant G/T snv 0.49 1
rs849298 7 107024402 intergenic variant T/A snv 0.58 1