Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 14
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 10
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 9
rs59332535
LMNA
0.827 0.160 1 156134911 missense variant G/A snv 5
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 5
rs74315379
TNNT2
0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 5
rs1553265736
LMNA
0.925 0.040 1 156136080 missense variant G/C snv 4
rs267607581
LMNA
0.925 0.080 1 156137651 splice region variant C/G snv 4
rs28933091
LMNA
0.882 0.160 1 156134474 missense variant C/A;G snv 4
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 4
rs727503512
TNNT2
0.851 0.080 1 201363349 missense variant G/A;C;T snv 4.0E-06 4
rs74315380
TNNT2
0.851 0.080 1 201364366 missense variant G/A;C snv 4
rs199476317
TPM1
0.827 0.080 15 63062263 missense variant G/A snv 4
rs397516881
BAG3
0.827 0.120 10 119676917 missense variant G/A snv 3
rs267607578
LMNA
0.925 0.120 1 156136952 missense variant G/A;C snv 1.4E-05 3
rs28933093
LMNA
0.882 0.160 1 156130741 missense variant G/A snv 3
rs397517889
LMNA
0.925 0.120 1 156136093 missense variant C/T snv 7.0E-06 3
rs56816490
LMNA
0.925 0.120 1 156135913 stop gained G/A;T snv 3
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 3
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 3
rs59684335
LMNA
0.882 0.120 1 156135280 frameshift variant CT/- delins 3
rs60890628
LMNA
0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 3
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 3
rs61672878
LMNA
0.776 0.200 1 156136094 missense variant G/A;T snv 3