Source: ALL

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: rs869736
rs869736
PTPRCAP ; CORO1B
0.925 0.080 11 67437991 3 prime UTR variant C/A snv 0.53
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs374535834
rs374535834
PTPRCAP ; RPS6KB2 ; CORO1B ; RPS6KB2-AS1
1.000 0.040 11 67435048 missense variant C/A;T snv 4.1E-06; 6.5E-05
CUI: C1335167
Disease: Ovarian Mucinous Adenocarcinoma
Ovarian Mucinous Adenocarcinoma 		0.700 0
dbSNP: rs756117196
rs756117196
PTPRCAP ; CORO1B
1.000 0.080 11 67438784 missense variant C/G;T snv 4.7E-06; 1.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 0
dbSNP: rs10274
rs10274
PTPRCAP ; RPS6KB2 ; CORO1B ; RPS6KB2-AS1
1.000 0.040 11 67435355 3 prime UTR variant G/A;T snv
CUI: C0014868
Disease: Esophagitis
Esophagitis 		0.010 1.000 1 2016 2016
dbSNP: rs869736
rs869736
PTPRCAP ; CORO1B
0.925 0.080 11 67437991 3 prime UTR variant C/A snv 0.53
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs869736
rs869736
PTPRCAP ; CORO1B
0.925 0.080 11 67437991 3 prime UTR variant C/A snv 0.53
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2009 2009