Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 9
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 1
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 14
rs386134243
LMNA
0.708 0.360 1 156135967 missense variant C/A;T snv 4.0E-06 16
rs45546039
SCN5A
0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 10
rs137854618
SCN5A
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 5
rs57077886
LMNA
0.776 0.240 1 156114947 missense variant C/T snv 3
rs60890628
LMNA
0.776 0.200 1 156138507 missense variant C/T snv 1.5E-04 1.0E-04 3
rs61672878
LMNA
0.776 0.200 1 156136094 missense variant G/A;T snv 3
rs60682848
LMNA
0.790 0.200 1 156134838 stop gained C/T snv 7.0E-06 4
rs150840924
LMNA
0.807 0.240 1 156136359 missense variant C/T snv 8.0E-06 7.0E-06 2
rs142000963
LMNA
0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 1
rs59332535
LMNA
0.827 0.160 1 156134911 missense variant G/A snv 5
rs74315379
TNNT2
0.827 0.080 1 201364336 missense variant G/A;T snv 1.2E-04 5
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
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 3
rs61195471
LMNA
0.827 0.160 1 156134496 missense variant G/A snv 3
rs59026483
LMNA
0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 2
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
rs121434420
PKP2
0.851 0.120 12 32879021 stop gained G/A snv 4.0E-06 4.9E-05 3
rs2856655
MYBPC3
0.851 0.080 11 47337534 missense variant C/G;T snv 2.0E-05 3
rs730882262
LMNA
0.851 0.160 1 156135293 missense variant T/C;G snv 3
rs61444459
LMNA
0.851 0.160 1 156137667 missense variant G/A;C snv 2