Source: UNIPROT ×
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: rs137854612
rs137854612
SCN5A
2 0.851 0.120 3 38560170 missense variant C/T snv 0.800 1.000 3 2001 2012
dbSNP: rs28937319
rs28937319
SCN5A
1 1.000 0.080 3 38562485 missense variant G/A snv 7.0E-06 0.800 1.000 3 2001 2012
dbSNP: rs45620037
rs45620037
SCN5A
2 0.882 0.120 3 38613787 missense variant G/A snv 6.6E-04 6.6E-04 0.800 0
dbSNP: rs137854611
rs137854611
SCN5A
2 0.882 0.120 3 38597787 missense variant G/A;C;T snv 4.0E-06 0.700 1.000 3 2001 2012
dbSNP: rs727504495
rs727504495
SCN5A
1 1.000 0.080 3 38550998 missense variant C/A;T snv 4.0E-06; 2.0E-05 0.700 0