Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs57920071
LMNA
0.763 0.320 1 156136984 missense variant C/T snv 4.0E-06 7.0E-06 11
rs61672878
LMNA
0.776 0.200 1 156136094 missense variant G/A;T snv 11
rs58034145
LMNA
0.827 0.160 1 156134830 missense variant A/C snv 10
rs57520892
LMNA
0.776 0.200 1 156137204 missense variant G/A;C snv 4.1E-05 8
rs58932704
LMNA
0.776 0.200 1 156136413 missense variant C/T snv 8
rs58912633
LMNA
0.851 0.240 1 156130688 missense variant C/G;T snv 5
rs60458016
LMNA
0.827 0.120 1 156136036 stop gained G/A;T snv 5
rs199474724
LMNA
0.851 0.120 1 156134839 missense variant G/A snv 4
rs267607545
LMNA
0.882 0.200 1 156136121 missense variant G/A;C;T snv 3
rs267607594
LMNA
0.925 0.120 1 156130745 missense variant T/C snv 3
rs28928901
LMNA
0.882 0.120 1 156134829 missense variant C/T snv 3
rs60934003
LMNA
0.882 0.160 1 156137213 missense variant T/C snv 3
rs1060502215
LMNA
0.925 0.120 1 156115040 missense variant G/A;T snv 2
rs58571998
LMNA
0.925 0.160 1 156137197 frameshift variant -/CTGC delins 2
rs59653062
LMNA
0.925 0.120 1 156136076 missense variant T/A snv 2