Disease: Arthritis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs3789604
RSBN1 ; AP4B1-AS1
0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs1234315
TNFSF4
0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs204991
GPSM3
0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs1477353313
ACR
0.925 0.120 22 50744085 missense variant T/G snv 2
rs204989
GPSM3
0.925 0.120 6 32194075 intron variant G/A snv 0.21 2