rs3807987, CAV1

N. diseases: 17
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.020 1.000 2 2017 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.020 1.000 2 2017 2019
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
278 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2011 2011
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
290 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2011 2011
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2013 2013
Infection caused by Helicobacter pylori
56 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2014 2014
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
167 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2011 2011
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
769 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2013 2013
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
172 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2011 2011
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
603 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2014 2014
Malignant neoplasm of urinary bladder
289 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2011 2011
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2013 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2013 2013
Sarcopenia
CUI: C0872084
Disease: Sarcopenia
10 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2015 2015
Squamous cell carcinoma of esophagus
320 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2014 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
616 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 0.010 1.000 1 2014 2014