Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs181126208
EDARADD
1.000 0.080 1 236495210 intron variant G/A snv 4.9E-02 2
rs2631781
ST6GALNAC3
1.000 0.080 1 76128101 intron variant C/A;T snv 2
rs6693796
PRRX1
1.000 0.080 1 170674137 intron variant T/C snv 7.7E-02 2
rs141864436
NRXN1
1.000 0.080 2 50971652 intron variant G/A snv 1.6E-02 2
rs145010525
DARS1
1.000 0.080 2 135975206 intron variant G/A snv 7.8E-03 2
rs4988198
MCM6
1.000 0.080 2 135861240 intron variant T/C;G snv 2
rs112284299
PEX5L
1.000 0.080 3 179850308 intron variant G/C snv 1.6E-02 2
rs115092681
NLGN1
1.000 0.080 3 174201323 intron variant G/A;C;T snv 2
rs115990514
LOC107986066
1.000 0.080 3 19055898 intergenic variant C/A snv 9.0E-03 2
rs13064411
CFAP44
3 113327793 synonymous variant A/G snv 0.12 9.9E-02 1
rs10034465
LINC02484
1.000 0.080 4 34193882 intron variant G/A snv 9.1E-02 2
rs6847878 1.000 0.080 4 81419698 intergenic variant G/T snv 9.1E-03 2
rs113816795 1.000 0.080 5 99159794 intergenic variant T/C snv 8.1E-03 2
rs75298135 1.000 0.080 5 28184372 intergenic variant A/C snv 1.3E-02 2
rs80333777
FBXL7
1.000 0.080 5 15524361 intron variant G/A;C;T snv 2
rs146807753 1.000 0.080 6 3904005 downstream gene variant C/A;T snv 2
rs75639901
SCGN
1.000 0.080 6 25667803 intron variant A/G snv 4.8E-02 2
rs9472719 1.000 0.080 6 46183649 regulatory region variant A/C snv 0.32 2
rs7810240
ZNF775
1.000 0.080 7 150387372 intron variant T/C;G snv 2
rs114007472 1.000 0.080 8 63563681 intergenic variant G/A snv 9.4E-03 2
rs34030778
CLN8
1.000 0.080 8 1771328 missense variant C/T snv 2.8E-03 1.1E-02 2
rs16914931
GABBR2
9 98330034 intron variant G/A snv 0.10 1
rs72804453
BICC1
1.000 0.080 10 58827232 intron variant A/G snv 2.0E-02 2
rs112209655
LOC102724680
1.000 0.080 12 84947358 intergenic variant C/T snv 1.0E-02 2
rs116616455 1.000 0.080 12 58041829 intergenic variant T/C snv 1.4E-02 2