CCNE1, cyclin E1, 898

N. diseases: 133; N. variants: 9
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: rs3218036
rs3218036
19 29814777 intron variant G/A snv 0.23
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs3218036
rs3218036
19 29814777 intron variant G/A snv 0.23
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs3218036
rs3218036
19 29814777 intron variant G/A snv 0.23
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs1406
rs1406
0.882 0.120 19 29824205 3 prime UTR variant C/A snv 0.28
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1406
rs1406
0.882 0.120 19 29824205 3 prime UTR variant C/A snv 0.28
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1406
rs1406
0.882 0.120 19 29824205 3 prime UTR variant C/A snv 0.28
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
Neoplasms; Stomatognathic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1406
rs1406
0.882 0.120 19 29824205 3 prime UTR variant C/A snv 0.28
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3218035
rs3218035
0.925 0.080 19 29814542 intron variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3218035
rs3218035
0.925 0.080 19 29814542 intron variant C/A;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3218038
rs3218038
0.882 0.120 19 29814988 intron variant G/T snv 9.1E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs3218038
rs3218038
0.882 0.120 19 29814988 intron variant G/T snv 9.1E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3218038
rs3218038
0.882 0.120 19 29814988 intron variant G/T snv 9.1E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3218038
rs3218038
0.882 0.120 19 29814988 intron variant G/T snv 9.1E-02
Secondary malignant neoplasm of lymph node
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs3218042
rs3218042
0.925 0.080 19 29816431 intron variant T/A snv 1.1E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3218042
rs3218042
0.925 0.080 19 29816431 intron variant T/A snv 1.1E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs3218073
rs3218073
0.882 0.160 19 29824109 3 prime UTR variant C/T snv 1.1E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs3218073
rs3218073
0.882 0.160 19 29824109 3 prime UTR variant C/T snv 1.1E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs3218073
rs3218073
0.882 0.160 19 29824109 3 prime UTR variant C/T snv 1.1E-02
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs3218073
rs3218073
0.882 0.160 19 29824109 3 prime UTR variant C/T snv 1.1E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs72010703
rs72010703
0.925 0.080 19 29813348 intron variant TTAG/-;TTAGTTAG delins
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs72010703
rs72010703
0.925 0.080 19 29813348 intron variant TTAG/-;TTAGTTAG delins
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs7257330
rs7257330
0.882 0.120 19 29810916 upstream gene variant G/A snv 0.30
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7257330
rs7257330
0.882 0.120 19 29810916 upstream gene variant G/A snv 0.30
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7257330
rs7257330
0.882 0.120 19 29810916 upstream gene variant G/A snv 0.30
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs997669
rs997669
0.925 0.080 19 29813576 intron variant T/C snv 0.30
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008