Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73975586
LOC101927727 ; NXN
0.776 0.080 17 911003 non coding transcript exon variant A/T snv 9.8E-02 10
rs4968127
NXN
0.776 0.080 17 906403 intron variant G/A;T snv 10
rs12603526
NXN
0.790 0.080 17 897353 intron variant T/C snv 2.3E-02 9
rs73975588
NXN
0.790 0.080 17 913501 intron variant A/C snv 9.9E-02 9