Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143558304
TPM4
19 16102887 3 prime UTR variant -/A delins 4.6E-02 2
rs11459029
ARHGEF3
3 56740187 intron variant -/A delins 1
rs3215853
DOCK8
9 273178 intron variant -/A delins 0.72 1
rs35547687 7 158833186 upstream gene variant -/A;AA delins 1
rs56990409 12 7989603 intergenic variant -/A;AA;AAAAAAA delins 1
rs11471957
TUBB1
20 59023277 intron variant -/AA ins 2
rs111896493
ADGRE5
19 14381256 5 prime UTR variant -/AGTG delins 1
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs532990872
PDS5B
13 32605907 intron variant -/TC ins 1
rs56318916
DOCK8
9 329344 intron variant A/- del 0.22 2
rs563151485
TAF7
5 141322493 intron variant A/- delins 6.6E-03 1
rs34061204
BANK1
4 101878992 intron variant A/-;AA;AAA delins 1
rs35383388
ACSL5
10 112391369 intron variant A/-;AA;AAA;AAAA delins 1
rs2393967
MIR1296 ; JMJD1C
10 63373396 intron variant A/C snv 0.23 3
rs80012730 12 49277876 upstream gene variant A/C snv 6.1E-02 2
rs10506328
NFE2
12 54293448 intron variant A/C snv 0.75 1
rs11950562
MIR3936HG ; SLC22A4
5 132316836 intron variant A/C snv 0.37 1
rs12102677
CBFA2T3 ; LOC100129697
16 88950086 intron variant A/C snv 0.34 1
rs80226907 14 55198171 intron variant A/C snv 5.8E-02 1
rs893001
CD226
18 69849610 intron variant A/C snv 0.18 1
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs987044
SSH1
12 108856580 intron variant A/C;G snv 1
rs75763843
LINC01478
18 44482415 intron variant A/C;T snv 2
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10