Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs8074026
SERPINF2
0.882 0.160 17 1753779 intron variant T/C snv 0.71 2
rs1460163 1.000 0.120 8 79315213 downstream gene variant G/A;T snv 1
rs295301 0.851 0.160 3 141619799 downstream gene variant G/A snv 0.38 1
rs6116492 1.000 0.120 20 4717980 upstream gene variant G/T snv 7.0E-02 1
rs7565981 1.000 0.120 2 100807869 intergenic variant G/A snv 0.15 1
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 1
rs4921542
MTMR7 ; LOC102724838
1.000 0.120 8 17348068 intron variant T/G snv 0.19 1
rs6107516
PRNP
1.000 0.120 20 4696446 intron variant G/A snv 0.23 1