Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434475
ND4 ; TRNG ; COX3 ; ND3 ; ND4L
1.000 0.080 MT 9997 non coding transcript exon variant T/C snv 1
rs199476321
TPM1
0.882 0.080 15 63064133 missense variant T/C snv 4.0E-06 1.4E-05 1
rs199476317
TPM1
0.827 0.080 15 63062263 missense variant G/A snv 4
rs199476316
TPM1
0.925 0.080 15 63062219 missense variant C/T snv 4.0E-06 7.0E-06 2
rs199476315
TPM1
0.827 0.080 15 63061723 missense variant G/A snv 4
rs104894502
TPM1
0.807 0.120 15 63060915 missense variant A/G;T snv 1
rs104894503
TPM1
0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 3
rs397516373
TPM1
0.925 0.080 15 63059663 missense variant G/A snv 4
rs1555408679
TPM1
1.000 0.080 15 63059648 missense variant A/G snv 1
rs727503506
TNNI3
1.000 0.080 19 55154743 missense variant C/G snv 8.0E-06 1
rs1568858210
TNNI3
1.000 0.080 19 55154175 missense variant A/G snv 1
rs730881069
TNNI3
1.000 0.080 19 55154172 missense variant C/T snv 4.0E-06 2
rs397516347
TNNI3
0.851 0.120 19 55154157 missense variant C/T snv 4.2E-05 3
rs104894724
TNNI3
0.790 0.120 19 55154146 missense variant G/A;C snv 4.0E-06 4
rs397516349
TNNI3
0.807 0.080 19 55154145 missense variant C/T snv 1.6E-05 6
rs397516353
TNNI3
0.882 0.080 19 55154109 missense variant G/A snv 3
rs368861241
TNNI3
0.851 0.120 19 55154095 missense variant G/A snv 4.0E-05 7.0E-06 3
rs397516354
TNNI3
0.790 0.120 19 55154094 missense variant C/A;G;T snv 4.0E-05 7
rs727504242
TNNI3
0.925 0.080 19 55154082 missense variant G/A snv 8.0E-06 7.0E-06 2
rs727503504
TNNI3
0.807 0.080 19 55154071 missense variant G/A;C snv 6
rs727503503
TNNI3
0.827 0.120 19 55154070 missense variant C/T snv 3
rs727503501
TNNI3
1.000 0.080 19 55154053 missense variant C/T snv 1
rs397516351
TNNI3
0.925 0.080 19 55154045 inframe deletion TTC/- delins 2
rs397516357
TNNI3
0.851 0.120 19 55151910 missense variant C/T snv 7.0E-06 3
rs104894729
TNNI3
0.827 0.080 19 55151892 missense variant C/A;G;T snv 4