Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs544838
NRXN2
0.925 0.120 11 64661587 intron variant T/C snv 0.52 3
rs490192
NRXN2
0.925 0.120 11 64703897 intron variant G/A snv 0.33 3
rs7932437
NRXN2
0.925 0.120 11 64606032 downstream gene variant T/C snv 0.52 3
rs504915
NRXN2
0.925 0.120 11 64696613 intron variant T/A;C snv 3
rs7117423
NRXN2-AS1 ; NRXN2
0.925 0.120 11 64657648 intron variant G/C;T snv 3
rs492175
NRXN2
0.925 0.120 11 64665606 intron variant G/A;C snv 2
rs2360873
NRXN2
0.925 0.120 11 64623685 non coding transcript exon variant G/C snv 0.49 2
rs11231845
NRXN2
0.925 0.120 11 64639947 intron variant G/A snv 0.51 2
rs471618
NRXN2
0.925 0.120 11 64697931 intron variant T/A;C;G snv 2
rs506338
NRXN2
0.925 0.120 11 64673448 intron variant T/C snv 0.52 2
rs10128590
NRXN2
0.925 0.120 11 64681953 intron variant G/A snv 0.26 2
rs10792443
NRXN2
0.925 0.120 11 64627780 intron variant G/C snv 0.51 2
rs480617
NRXN2
0.925 0.120 11 64710848 intron variant C/T snv 0.57 2
rs948689
NRXN2
0.925 0.120 11 64633247 intron variant A/G;T snv 2
rs7121121
NRXN2
0.925 0.120 11 64613660 intron variant T/C snv 0.33 2
rs519090
NRXN2
0.925 0.120 11 64688768 intron variant G/C snv 0.49 2
rs17146216
NRXN2
0.925 0.120 11 64683809 intron variant C/G snv 0.23 2
rs551890
NRXN2
0.925 0.120 11 64710527 intron variant C/T snv 0.73 2
rs11602411
NRXN2
0.925 0.120 11 64681751 intron variant G/A snv 0.11 2
rs2277311
NRXN2
0.925 0.120 11 64620460 intron variant G/A snv 0.49 2
rs500531
NRXN2
0.925 0.120 11 64719547 intron variant G/T snv 0.50 2
rs2666559
NRXN2
0.925 0.120 11 64671755 intron variant G/A;T snv 2
rs1207226
NRXN2
0.925 0.120 11 64634555 intron variant T/C snv 0.33 2
rs530252
NRXN2
0.925 0.120 11 64675993 non coding transcript exon variant T/C snv 0.33 2
rs4930556
NRXN2
0.925 0.120 11 64610254 intron variant G/C snv 0.52 2