Source: BEFREE

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: rs4143815
rs4143815
CD274
0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs2890658
rs2890658
CD274
0.925 0.080 9 5465130 intron variant C/A;T snv
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.010 1.000 1 2017 2017
dbSNP: rs4143815
rs4143815
CD274
0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.010 1.000 1 2017 2017
dbSNP: rs4143815
rs4143815
CD274
0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs4143815
rs4143815
CD274
0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23
CUI: C1720771
Disease: Testicular Hydrocele
Testicular Hydrocele 		0.010 1.000 1 2019 2019