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: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C0025286
Disease: Meningioma
Meningioma 		0.020 1.000 2 2008 2018
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma 		0.020 1.000 2 2008 2018
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
Meningioma, benign, no ICD-O subtype 		0.020 1.000 2 2008 2018
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2013 2013
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C1512260
Disease: Grade I Meningioma
Grade I Meningioma 		0.010 1.000 1 2018 2018
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2018 2018
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2008 2008
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C2347751
Disease: Adult Grade I Meningioma
Adult Grade I Meningioma 		0.010 1.000 1 2018 2018
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C2347760
Disease: Childhood Grade I Meningioma
Childhood Grade I Meningioma 		0.010 1.000 1 2018 2018
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C0334611
Disease: Transitional Meningioma
Transitional Meningioma 		0.010 1.000 1 2018 2018
dbSNP: rs4968451
rs4968451
BRIP1
0.732 0.160 17 61849946 intron variant A/C snv 0.15
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2013 2013