Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs762513613
FCGR2C
0.752 0.280 1 161591315 missense variant A/G snv 4.2E-06 7.4E-06 11
rs1308699981
FCGR3A
0.807 0.440 1 161543085 missense variant G/A snv 4.0E-06 7
rs1161169998
TNFSF13B
1.000 0.120 13 108303360 missense variant G/A snv 7.0E-06 1
rs146436713
TNFRSF13B
1.000 0.120 17 16948957 missense variant C/A;T snv 8.0E-06; 1.9E-04 1
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs879761216
CNR2
0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10