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: rs58262369
rs58262369
0.925 0.080 14 64227194 3 prime UTR variant C/T snv 2.4E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.710 1.000 1 2015 2015
dbSNP: rs1256049
rs1256049
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.040 0.500 4 2005 2018
dbSNP: rs1256049
rs1256049
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.040 0.500 4 2005 2018
dbSNP: rs1256049
rs1256049
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.030 1.000 3 2012 2015
dbSNP: rs1256049
rs1256049
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 1.000 3 2012 2015
dbSNP: rs1271572
rs1271572
0.708 0.400 14 64295199 intron variant A/C;T snv
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.030 1.000 3 2009 2018
dbSNP: rs1271572
rs1271572
0.708 0.400 14 64295199 intron variant A/C;T snv
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.030 1.000 3 2009 2018
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.030 1.000 3 2009 2015
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 0.667 3 2005 2014
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.030 0.667 3 2005 2014
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 1.000 3 2009 2015
dbSNP: rs1256049
rs1256049
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02
CUI: C0021364
Disease: Male infertility
Male infertility
0.020 1.000 2 2009 2014
dbSNP: rs1256049
rs1256049
0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.020 1.000 2 2012 2014
dbSNP: rs1256120
rs1256120
0.882 0.200 14 64338283 non coding transcript exon variant A/G snv 0.20
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
0.020 1.000 2 2011 2017
dbSNP: rs1271572
rs1271572
0.708 0.400 14 64295199 intron variant A/C;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 1.000 2 2007 2008
dbSNP: rs1271572
rs1271572
0.708 0.400 14 64295199 intron variant A/C;T snv
CUI: C0029925
Disease: Ovarian Carcinoma
Ovarian Carcinoma
0.020 1.000 2 2009 2011
dbSNP: rs1271572
rs1271572
0.708 0.400 14 64295199 intron variant A/C;T snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.020 1.000 2 2011 2018
dbSNP: rs3020450
rs3020450
0.807 0.200 14 64301584 splice region variant C/A;T snv
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.020 1.000 2 2018 2019
dbSNP: rs3020450
rs3020450
0.807 0.200 14 64301584 splice region variant C/A;T snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.020 1.000 2 2018 2019
dbSNP: rs3020450
rs3020450
0.807 0.200 14 64301584 splice region variant C/A;T snv
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.020 1.000 2 2018 2019
dbSNP: rs3020450
rs3020450
0.807 0.200 14 64301584 splice region variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 < 0.001 2 2014 2019
dbSNP: rs3020450
rs3020450
0.807 0.200 14 64301584 splice region variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 < 0.001 2 2014 2019
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular
0.020 1.000 2 2009 2012
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.020 1.000 2 2011 2018
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 1.000 2 2009 2012