Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1331308
HBS1L
6 135083984 intron variant A/C snv 0.61 1
rs4731120
HYAL4
7 123771169 intergenic variant A/C snv 6.5E-02 1
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 2
rs4326844
COPZ1
12 54342686 intron variant A/C;G snv 0.68 1
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs10974808
RCL1
9 4840380 intron variant A/G snv 9.0E-02 2
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 2
rs513349
GGNBP1 ; BAK1
1.000 0.120 6 33573942 intron variant A/G snv 0.51 0.51 2
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 2
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 2
rs151361
PRELID3B ; SLMO2-ATP5E
20 59038947 intron variant A/G snv 0.24 1
rs1719271 15 64891602 intron variant A/G snv 0.20 1
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 1
rs3809566
TPM1
15 63041525 upstream gene variant A/G snv 0.69 1
rs4148441
ABCC4
13 95245953 intron variant A/G snv 0.91 1
rs4470077
LOC107984664 ; TBPL2
14 55430820 intron variant A/G snv 0.29 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs625132
EHD3
2 31259434 intron variant A/G snv 0.82 1
rs7616006 3 12226148 intergenic variant A/G snv 0.48 1
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 1
rs8006385
ITPK1
14 93034681 intron variant A/G snv 0.13 1
rs457287
RCL1
9 4834394 intron variant A/G;T snv 1
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 2