Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6800541
SCN10A
1.000 0.080 3 38733341 intron variant C/T snv 0.70 2
rs11708996
SCN5A
0.925 0.120 3 38592432 intron variant G/C snv 0.11 5