Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7752643
SNAP91
1.000 0.040 6 83570556 intron variant C/A;G;T snv 2
rs91894
SNAP91
1.000 0.040 6 83678186 intron variant C/G snv 0.37 2
rs217287
SNAP91
1.000 0.040 6 83697747 intron variant C/T snv 0.36 1
rs217331
SNAP91
1.000 0.040 6 83634970 intron variant G/C;T snv 1
rs3798869
SNAP91
1.000 0.040 6 83618941 intron variant G/A snv 0.37 1