TAGLN, transgelin, 6876

N. diseases: 131; N. variants: 4
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: rs508487
rs508487 		11 117204850 3 prime UTR variant C/T snv 5.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 4 2011 2019
dbSNP: rs17120434
rs17120434 		11 117204969 3 prime UTR variant A/G;T snv 5.4E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17120434
rs17120434 		11 117204969 3 prime UTR variant A/G;T snv 5.4E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17120434
rs17120434 		11 117204969 3 prime UTR variant A/G;T snv 5.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs508487
rs508487 		11 117204850 3 prime UTR variant C/T snv 5.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs508487
rs508487 		11 117204850 3 prime UTR variant C/T snv 5.2E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs508487
rs508487 		11 117204850 3 prime UTR variant C/T snv 5.2E-02
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement 		0.700 1.000 1 2011 2011
dbSNP: rs641620
rs641620 		11 117203513 intron variant T/C snv 0.27 0.27
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs74949440
rs74949440 		0.925 0.080 11 117199645 5 prime UTR variant C/G;T snv 1.9E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs74949440
rs74949440 		0.925 0.080 11 117199645 5 prime UTR variant C/G;T snv 1.9E-02
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm 		Neoplasms 0.700 1.000 1 2017 2017