Disease: Viral Load result
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 7
rs1015164
CCRL2
0.925 3 46410189 intron variant A/C;G;T snv 6
rs10039039
KCNIP1
1.000 5 170487960 intron variant C/T snv 8.9E-02 5
rs1005585
CBS
1.000 21 43056923 intron variant T/C snv 6.5E-02 5
rs10182825
PPP1CB ; SPDYA
1.000 2 28788221 intron variant G/A snv 9.0E-02 5
rs10467472
RGCC
1.000 13 41459562 intron variant G/C;T snv 5
rs113974007 1.000 1 244750932 intergenic variant T/C snv 7.3E-02 5
rs11905359
TMEM230
1.000 20 5079306 intron variant C/A snv 7.1E-02 5
rs11933652 1.000 4 28961215 intergenic variant T/C snv 0.12 5
rs12532102
CDCA7L
1.000 7 21927090 intron variant A/G snv 0.82 5
rs13391004 1.000 2 136609937 intergenic variant G/A snv 9.1E-02 5
rs1349596
CADPS
1.000 3 62542448 intron variant C/T snv 6.3E-02 5
rs148332376
RHOH
1.000 4 40240870 intron variant -/T delins 7.0E-02 5
rs150933152
CLEC18B
1.000 16 74411734 missense variant C/T snv 5
rs17029090
C4orf17
1.000 4 99522696 synonymous variant A/G snv 4.8E-02 8.8E-02 5
rs17079875
RNF130
1.000 5 179974542 intron variant G/A snv 6.8E-02 5
rs17160151
FBN3
1.000 19 8085509 missense variant C/T snv 1.8E-02 7.3E-02 5
rs17171670
SUGCT ; LOC105375245
1.000 7 40294343 intron variant T/G snv 8.1E-02 5
rs17841547 1.000 16 35734888 upstream gene variant A/C;G snv 5
rs1868175
SLC9A9
1.000 3 143686482 intron variant A/G snv 0.75 5
rs2070715
FGF1 ; SPRY4-AS1
1.000 5 142644691 intron variant T/C;G snv 5
rs2157999
CUX2
1.000 12 111266635 intron variant G/A snv 8.1E-02 5
rs217514
CREB5
1.000 7 28506192 intron variant T/C snv 0.27 5
rs2505447
LINC00836
1.000 10 25728984 intron variant A/G;T snv 5
rs2514923
LINC02748
1.000 11 91221441 intron variant C/G;T snv 5