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: rs397516354
rs397516354
TNNI3
8 0.790 0.120 19 55154094 missense variant C/A;G;T snv 4.0E-05 0.800 1.000 10 1997 2012
dbSNP: rs104894724
rs104894724
TNNI3
8 0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 0.800 1.000 9 1997 2017
dbSNP: rs104894725
rs104894725
TNNI3
3 0.882 0.080 19 55151851 missense variant T/C;G snv 0.800 1.000 9 1997 2017
dbSNP: rs104894727
rs104894727
TNNI3
4 0.882 0.080 19 55151881 missense variant C/A;T snv 4.0E-06 0.800 1.000 9 1997 2017
dbSNP: rs397516353
rs397516353
TNNI3
3 0.882 0.080 19 55154109 missense variant G/A snv 0.800 1.000 9 1997 2017
dbSNP: rs727504242
rs727504242
TNNI3
2 0.925 0.080 19 55154082 missense variant G/A snv 8.0E-06 7.0E-06 0.800 1.000 4 2011 2017
dbSNP: rs368861241
rs368861241
TNNI3
4 0.851 0.120 19 55154095 missense variant G/A snv 4.0E-05 7.0E-06 0.700 1.000 6 2000 2014
dbSNP: rs397516347
rs397516347
TNNI3
5 0.851 0.120 19 55154157 missense variant C/T snv 4.2E-05 0.700 1.000 5 1997 2005
dbSNP: rs397516357
rs397516357
TNNI3
5 0.851 0.120 19 55151910 missense variant C/T snv 7.0E-06 0.700 1.000 5 1997 2005
dbSNP: rs104894728
rs104894728
TNNI3
2 0.925 0.040 19 55151898 missense variant T/C snv 0.700 0
dbSNP: rs267607127
rs267607127
TNNI3
3 0.882 0.120 19 55151860 missense variant C/T snv 0.700 0
dbSNP: rs267607128
rs267607128
TNNI3
3 0.882 0.040 19 55157097 missense variant G/A snv 0.700 0
dbSNP: rs397516349
rs397516349
TNNI3
6 0.807 0.080 19 55154145 missense variant C/T snv 1.6E-05 0.700 0
dbSNP: rs727503504
rs727503504
TNNI3
6 0.807 0.080 19 55154071 missense variant G/A;C snv 0.700 0
dbSNP: rs727504275
rs727504275
TNNI3
2 0.925 0.040 19 55151856 missense variant C/A;T snv 4.0E-06 0.700 0