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: rs2612656
rs2612656
HPGD
1.000 0.080 4 174501138 intron variant G/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs8752
rs8752
HPGD
0.827 0.160 4 174491326 3 prime UTR variant C/T snv 0.49
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2014 2014
dbSNP: rs8752
rs8752
HPGD
0.827 0.160 4 174491326 3 prime UTR variant C/T snv 0.49
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs8752
rs8752
HPGD
0.827 0.160 4 174491326 3 prime UTR variant C/T snv 0.49
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs8752
rs8752
HPGD
0.827 0.160 4 174491326 3 prime UTR variant C/T snv 0.49
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs8752
rs8752
HPGD
0.827 0.160 4 174491326 3 prime UTR variant C/T snv 0.49
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2017 2017