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: rs13376333
rs13376333
KCNN3
2 0.925 0.080 1 154841877 intron variant C/T snv 0.28 0.020 1.000 2 2012 2014
dbSNP: rs2200733
rs2200733 		12 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 0.020 1.000 2 2011 2011
dbSNP: rs10465885
rs10465885
GJA5 ; LOC102723321
4 0.882 0.080 1 147760632 intron variant T/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs1131820
rs1131820
KCNN3
2 0.925 0.080 1 154772376 synonymous variant A/G snv 0.77 0.71 0.010 1.000 1 2014 2014
dbSNP: rs121434557
rs121434557
GJA5 ; LOC102723321
4 0.882 0.200 1 147758953 missense variant C/A;T snv 1.2E-04 2.0E-04 0.010 1.000 1 2013 2013
dbSNP: rs202117321
rs202117321
KCNA5
1 1.000 0.080 12 5044611 missense variant A/G snv 7.2E-05 7.0E-05 0.010 1.000 1 2017 2017
dbSNP: rs2106809
rs2106809
ACE2
8 0.827 0.120 X 15599938 intron variant A/G snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs3825214
rs3825214
TBX5
8 0.851 0.080 12 114357638 intron variant G/A snv 0.77 0.010 1.000 1 2013 2013
dbSNP: rs6590357
rs6590357
KCNJ5 ; C11orf45
3 0.882 0.120 11 128911444 synonymous variant T/C snv 0.84 0.85 0.010 1.000 1 2011 2011
dbSNP: rs7118824
rs7118824
KCNJ5
1 1.000 0.080 11 128912083 synonymous variant T/A;G snv 0.84 0.010 1.000 1 2011 2011
dbSNP: rs773287275
rs773287275
KCNE3
1 1.000 0.080 11 74457515 missense variant C/T snv 4.8E-05 2.1E-05 0.010 1.000 1 2008 2008