Source: ALL
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: rs137854618
rs137854618
SCN5A
15 0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 0.700 1.000 2 2003 2013
dbSNP: rs121434557
rs121434557
GJA5 ; LOC102723321
4 0.882 0.200 1 147758953 missense variant C/A;T snv 1.2E-04 2.0E-04 0.700 0
dbSNP: rs121434558
rs121434558
GJA5 ; LOC102723321
3 0.882 0.120 1 147758977 missense variant G/A snv 0.700 0