Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6059655
rs6059655
0.790 0.080 20 34077942 intron variant A/G snv 0.95
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs6743068
rs6743068
1.000 0.040 2 201289197 intron variant A/G snv 0.72
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs405509
rs405509
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs3846662
rs3846662
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs1460816
rs1460816
1.000 0.040 13 32354271 intron variant G/A snv 0.54
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs2494938
rs2494938
0.752 0.240 6 40568389 intron variant G/A snv 0.51
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.800 1.000 1 2012 2012
dbSNP: rs12916300
rs12916300
0.742 0.080 15 28165345 intron variant C/T snv 0.50
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs6791479
rs6791479
1.000 0.040 3 189487243 intergenic variant T/A snv 0.48
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs2285947
rs2285947
0.807 0.120 7 21544470 intron variant G/A snv 0.44
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.800 1.000 1 2012 2012
dbSNP: rs2239815
rs2239815
0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs11707807
rs11707807
LPP
1.000 0.040 3 188370473 intron variant A/G snv 0.36
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs7242481
rs7242481
0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2013 2013
dbSNP: rs1246946
rs1246946
0.851 0.040 6 4979722 downstream gene variant C/T snv 0.34
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs4822983
rs4822983
0.925 0.080 22 28719078 intron variant C/T snv 0.33
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs8063761
rs8063761
1.000 0.040 16 89961218 intron variant A/T snv 0.33
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs2847281
rs2847281
1.000 0.040 18 12821594 intron variant A/G snv 0.32
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs1050631
rs1050631
0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.800 1.000 1 2013 2013
dbSNP: rs4268748
rs4268748
0.925 0.080 16 89960104 intron variant T/C snv 0.30
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs17761864
rs17761864
1.000 0.040 17 2268343 intron variant C/A snv 0.28
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2012 2012
dbSNP: rs754626
rs754626
SRC
0.925 0.080 20 37388937 intron variant T/G snv 0.25
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs9383064
rs9383064
1.000 0.040 6 15535090 intron variant G/C snv 0.24
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs4761496
rs4761496
0.851 0.040 12 94733833 regulatory region variant T/A;C snv 0.23
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2017 2017
dbSNP: rs4455710
rs4455710
1.000 0.040 6 32641081 intron variant C/T snv 0.22
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs13301660
rs13301660
1.000 0.040 9 136446350 intron variant C/T snv 0.20
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2019 2019