rs6800541, SCN10A

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Electrocardiogram: P-R interval
CUI: C0429087
Disease: Electrocardiogram: P-R interval
138 1.000 0.080 3 38733341 intron variant C/T snv 0.70 0.800 1.000 3 2010 2019
Heart Function Tests
CUI: C0018803
Disease: Heart Function Tests
27 1.000 0.080 3 38733341 intron variant C/T snv 0.70 0.700 1.000 1 2010 2010
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 1.000 0.080 3 38733341 intron variant C/T snv 0.70 0.020 1.000 2 2015 2017