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: rs267607129
rs267607129
TNNI3
2 0.925 0.040 19 55151912 missense variant G/C snv 0.800 1.000 2 2009 2012
dbSNP: rs267607130
rs267607130
TNNI3
2 0.925 0.040 19 55157052 missense variant T/G snv 0.800 1.000 2 2009 2012
dbSNP: rs397516354
rs397516354
TNNI3
8 0.790 0.120 19 55154094 missense variant C/A;G;T snv 4.0E-05 0.700 1.000 5 2003 2012
dbSNP: rs777177571
rs777177571
TNNI3
1 1.000 0.040 19 55154766 missense variant G/C snv 1.6E-05 2.1E-05 0.700 1.000 2 2009 2012
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