Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs6490294
ACAD10
12 111752634 intron variant C/A snv 0.35 1
rs35383388
ACSL5
10 112391369 intron variant A/-;AA;AAA;AAAA delins 1
rs146605626
ACSL5
10 112394994 synonymous variant G/A snv 1.5E-02 1.5E-02 1
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 7
rs1001494
ST7L
1 112567997 intron variant T/C snv 0.50 1
rs7317038
GRTP1-AS1 ; GRTP1
13 113358583 intron variant C/T snv 0.34 1
rs4907622
GRTP1
13 113362571 intron variant G/C;T snv 3
rs57567837 13 113370553 intergenic variant T/C snv 3.5E-02 1
rs2271494
SIDT1
3 113581336 intron variant A/T snv 0.46 0.46 1
rs73000929
ZBTB16
11 114082900 intron variant G/A;T snv 2.1E-02 2
rs17116384
ZBTB16
11 114110519 intron variant A/G snv 0.25 3
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs13228847
CAPZA2
7 116904931 intron variant G/A;T snv 1
rs34344826
TESC
12 117040963 intron variant CTC/-;CTCCTC delins 1
rs35986908
TENT5C
1 117608080 intron variant AA/-;A;AAA;AAAA;AAAAA;AAAAAAA delins 1
rs118033845 10 11794093 TF binding site variant G/A snv 2.6E-02 1
rs11593377
PROSER2-AS1 ; PROSER2
10 11853098 intron variant T/C;G snv 1
rs7743045
SELENOKP3
6 118781108 intron variant A/G snv 0.65 1
rs10886430
GRK5
10 119250744 intron variant A/G snv 8.8E-02 3
rs4849845
RALB
2 120255593 intron variant G/A snv 0.71 1
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs34818942
LOC107984442 ; RHOF
12 121789928 intron variant C/A;T snv 1
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13