Source: UNIPROT

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: rs116150891
rs116150891
CDKN2A
1.000 0.040 9 21970929 missense variant G/A;C snv 5.6E-04 2.6E-03
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 0
dbSNP: rs121913082
rs121913082
FAS
1.000 0.040 10 89014205 missense variant A/G snv
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 0
dbSNP: rs121913083
rs121913083
FAS
1.000 0.040 10 89008907 missense variant A/G snv
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 0
dbSNP: rs121913084
rs121913084
FAS
1.000 0.040 10 89010779 missense variant T/C snv
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 0
dbSNP: rs201125580
rs201125580
PTCH1 ; LOC100507346
1.000 0.040 9 95467191 missense variant C/A;T snv 4.0E-06; 3.8E-04
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 0
dbSNP: rs6413464
rs6413464
CDKN2A
1.000 0.040 9 21970980 missense variant C/A;G snv 1.3E-03; 4.1E-06
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 0
dbSNP: rs779417284
rs779417284
PTCH1
1.000 0.040 9 95449149 missense variant C/T snv 2.4E-05
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 0