Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73391993
STAB2
1.000 12 103592748 intron variant G/T snv 2.5E-02 1
rs57997684
ELOVL2
1.000 6 11014323 intron variant A/C snv 0.13 1
rs192238733
CELF2
1.000 10 11109944 intron variant G/A snv 4.1E-03 1
rs114830967
DPP10
1.000 2 115820465 intron variant C/T snv 2.0E-02 1
rs77063336
ASTN2
1.000 9 116932295 intron variant C/T snv 3.3E-02 1
rs4767831
LOC105370027 ; TMEM233
1.000 12 119601623 intron variant A/C;G snv 1
rs10505380
COL14A1
1.000 8 120314234 intron variant A/G snv 0.14 1
rs116502295
ETS1
1.000 11 128462620 intron variant T/C snv 6.1E-03 7.1E-03 1
rs78147979
ST14
1.000 11 130175205 intron variant G/A snv 1.0E-02 1
rs211437
EYA4
1.000 6 133292270 intron variant T/C snv 4.0E-02 1
rs12232685
LDLRAD4
1.000 18 13437028 intron variant C/T snv 4.8E-02 1
rs7048567
ABCA2
1.000 9 137009585 synonymous variant A/G snv 0.68 0.70 1
rs1882642
LRP1B
1.000 2 141104341 intron variant A/G;T snv 1
rs72700531
NFIB
1.000 9 14346344 intron variant C/T snv 1.3E-02 1
rs7721607
FBXL7
1.000 5 15652449 intron variant G/A snv 0.17 1
rs7087342
ADARB2
1.000 10 1613599 intron variant G/A snv 0.11 1
rs61806081
KIFAP3
1.000 1 169931786 intron variant G/A snv 1.1E-02 1
rs138288216
NLGN1
1.000 3 174250679 intron variant G/T snv 7.1E-03 1
rs3775578
IRF2
1.000 4 184451980 intron variant T/C snv 0.16 1
rs73184656
LOC100131635 ; BCL6
1.000 3 187724028 intron variant A/C snv 0.18 1
rs142897541
TMEFF2
1.000 2 192095144 intron variant C/T snv 1.6E-02 1
rs146425640
NAV2
1.000 11 19823052 intron variant A/C snv 2.8E-03 1
rs12118495
SOX13
1.000 1 204077651 intron variant C/T snv 7.8E-02 1
rs3800917
MAD1L1
1.000 7 2128304 intron variant G/A snv 0.28 1
rs150859230
ESRRG
1.000 1 216675108 intron variant C/T snv 1.4E-02 1