rs4968451, BRIP1

N. diseases: 13
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.020 1.000 2 2008 2018
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.020 1.000 2 2008 2018
Meningioma, benign, no ICD-O subtype
30 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.020 1.000 2 2008 2018
Adult Grade I Meningioma
CUI: C2347751
Disease: Adult Grade I Meningioma
1 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2018 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2008 2008
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2013 2013
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2013 2013
Childhood Grade I Meningioma
CUI: C2347760
Disease: Childhood Grade I Meningioma
1 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2018 2018
Grade I Meningioma
CUI: C1512260
Disease: Grade I Meningioma
1 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2018 2018
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2008 2008
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2013 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2018 2018
Transitional Meningioma
CUI: C0334611
Disease: Transitional Meningioma
1 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.010 1.000 1 2018 2018