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: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 < 0.001 1 2009 2009
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2012 2012
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 < 0.001 1 2009 2009
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		0.010 1.000 1 2009 2009
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		0.010 1.000 1 2009 2009
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.010 1.000 1 2009 2009
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2010 2010
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2013 2013
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 < 0.001 1 2009 2009
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2013 2013
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia 		0.010 1.000 1 2010 2010
dbSNP: rs2075686
rs2075686
XRCC4 ; TMEM167A
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2010 2010