NCOA3, nuclear receptor coactivator 3, 8202

N. diseases: 142; N. variants: 5
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2076546
rs2076546
0.925 0.080 20 47639749 synonymous variant A/G snv 9.2E-02 0.13
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2076546
rs2076546
0.925 0.080 20 47639749 synonymous variant A/G snv 9.2E-02 0.13
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2230782
rs2230782
0.925 0.080 20 47636144 missense variant G/A;C snv 2.8E-05; 7.1E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2230782
rs2230782
0.925 0.080 20 47636144 missense variant G/A;C snv 2.8E-05; 7.1E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2425955
rs2425955
20 47540255 intron variant G/T snv 0.47
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6066394
rs6066394
1.000 0.040 20 47581409 intron variant C/T snv 0.29
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6066394
rs6066394
1.000 0.040 20 47581409 intron variant C/T snv 0.29
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6094753
rs6094753
20 47630030 intron variant G/A snv 0.47
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015