Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs104894002
LOC105375056 ; TREM2
0.790 0.320 6 41161557 stop gained G/A snv 2.0E-05 2.1E-05 5
rs2234253
TREM2 ; LOC105375056
0.827 0.120 6 41161367 missense variant G/A;C;T snv 1.9E-04; 1.0E-02 5
rs753325601
TREM2 ; LOC105375056
0.851 0.200 6 41161515 missense variant G/A snv 2.8E-05 7.0E-06 4
rs2234256
TREML1 ; LOC105375056 ; TREM2
0.882 0.120 6 41158917 missense variant A/G snv 1.8E-02 4.0E-02 3
rs766647311
TREML1 ; LOC105375056 ; TREM2
0.882 0.080 6 41159841 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs121908402
TREM2 ; LOC105375056
0.882 0.280 6 41161277 missense variant A/C snv 1.2E-05 1
rs142232675
TREM2 ; LOC105375056
1.000 0.080 6 41161395 missense variant C/T snv 9.7E-04 1.5E-03 1
rs143332484
TREM2 ; LOC105375056
1.000 0.080 6 41161469 missense variant C/A;T snv 7.6E-03 1
rs201280312
TREM2 ; LOC105375056
1.000 0.080 6 41161265 missense variant G/A snv 8.0E-06 1
rs150277350
TREM2 ; LOC105375056 ; TREML1
1.000 0.080 6 41158975 missense variant C/T snv 1.4E-04 9.8E-05 1
rs149622783
TREM2 ; TREML1 ; LOC105375056
1.000 0.080 6 41159867 missense variant C/G;T snv 4.0E-06; 1.2E-04 1
rs2234255
TREM2 ; TREML1 ; LOC105375056
1.000 0.080 6 41159805 missense variant G/A snv 4.9E-03 1.8E-03 1