Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9472719 1.000 0.080 6 46183649 regulatory region variant A/C snv 0.32 2
rs80147136 1.000 0.080 16 47050042 intergenic variant C/A snv 0.11 2
rs141864436
NRXN1
1.000 0.080 2 50971652 intron variant G/A snv 1.6E-02 2
rs116616455 1.000 0.080 12 58041829 intergenic variant T/C snv 1.4E-02 2
rs72804453
BICC1
1.000 0.080 10 58827232 intron variant A/G snv 2.0E-02 2
rs114007472 1.000 0.080 8 63563681 intergenic variant G/A snv 9.4E-03 2
rs2631781
ST6GALNAC3
1.000 0.080 1 76128101 intron variant C/A;T snv 2
rs6847878 1.000 0.080 4 81419698 intergenic variant G/T snv 9.1E-03 2
rs73354145
MRPL12
1.000 0.080 17 81706393 intron variant C/T snv 5.1E-02 2
rs112209655
LOC102724680
1.000 0.080 12 84947358 intergenic variant C/T snv 1.0E-02 2
rs16914931
GABBR2
9 98330034 intron variant G/A snv 0.10 1
rs113816795 1.000 0.080 5 99159794 intergenic variant T/C snv 8.1E-03 2