Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10428132
rs10428132
SCN10A
1 0.925 0.120 3 38736063 intron variant T/G snv 0.67 0.830 1.000 1 2013 2018
dbSNP: rs9388451
rs9388451 		1 0.882 0.120 6 125769231 regulatory region variant T/A;C snv 0.830 1.000 1 2013 2017
dbSNP: rs11708996
rs11708996
SCN5A
5 0.925 0.120 3 38592432 intron variant G/C snv 0.11 0.820 1.000 1 2013 2018