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: rs199473122
rs199473122
SCN5A
1 1.000 0.080 3 38603973 missense variant A/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473143
rs199473143
SCN5A
3 0.925 0.080 3 38597949 missense variant T/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473154
rs199473154
SCN5A
1 1.000 0.080 3 38587563 missense variant C/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473156
rs199473156
SCN5A
1 1.000 0.080 3 38587545 missense variant A/C;G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473158
rs199473158
SCN5A
1 1.000 0.080 3 38587519 missense variant G/A;T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473164
rs199473164
SCN5A
1 1.000 0.080 3 38585962 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473169
rs199473169
SCN5A
2 0.925 0.080 3 38585821 missense variant T/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473170
rs199473170
SCN5A
1 1.000 0.080 3 38585804 missense variant A/G;T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473173
rs199473173
SCN5A
1 1.000 0.080 3 38585792 missense variant A/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473174
rs199473174
SCN5A
1 1.000 0.080 3 38585777 stop gained C/A;T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473176
rs199473176
SCN5A
1 1.000 0.080 3 38585728 missense variant A/C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473178
rs199473178
SCN5A
1 1.000 0.080 3 38585695 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473179
rs199473179
SCN5A
1 1.000 0.080 3 38581355 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473199
rs199473199
SCN5A
1 1.000 0.080 3 38576753 missense variant C/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473208
rs199473208
SCN5A
1 1.000 0.080 3 38566541 missense variant C/A snv 0.700 1.000 21 1998 2016
dbSNP: rs199473213
rs199473213
SCN5A
1 1.000 0.080 3 38566503 missense variant A/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473214
rs199473214
SCN5A
1 1.000 0.080 3 38566491 missense variant T/C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473217
rs199473217
SCN5A
1 1.000 0.080 3 38562515 missense variant G/C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473219
rs199473219
SCN5A
1 1.000 0.080 3 38562446 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473221
rs199473221
SCN5A
1 1.000 0.080 3 38560424 missense variant A/C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473225
rs199473225
SCN5A
6 0.851 0.120 3 38560397 missense variant G/A;C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473228
rs199473228
SCN5A
1 1.000 0.080 3 38560362 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473229
rs199473229
SCN5A
4 0.882 0.120 3 38560361 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473230
rs199473230
SCN5A
1 1.000 0.080 3 38560356 missense variant G/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473231
rs199473231
SCN5A
1 1.000 0.080 3 38560355 missense variant A/G snv 0.700 1.000 21 1998 2016