Source: ALL

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: rs4778636
rs4778636
IL16
15 81299298 splice region variant G/A snv 0.10 0.12
CUI: C2697764
Disease: Interleukin 16 Measurement
Interleukin 16 Measurement 		0.700 1.000 2 2017 2017
dbSNP: rs11072996
rs11072996
IL16
15 81237069 intron variant C/T snv 0.95
CUI: C2697764
Disease: Interleukin 16 Measurement
Interleukin 16 Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs11325
rs11325
IL16 ; STARD5
15 81308999 3 prime UTR variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs11556218
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2017 2017
dbSNP: rs17875533
rs17875533
IL16
15 81305884 non coding transcript exon variant C/A snv 9.6E-02 0.12
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs28648707
rs28648707
IL16
15 81241693 intron variant G/A;T snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs4448892
rs4448892
IL16
15 81196722 intron variant C/T snv 0.30
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4778639
rs4778639
IL16
15 81308110 intron variant T/G snv 5.9E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs67093094
rs67093094
IL16
15 81238507 intron variant C/T snv 0.15
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs7166271
rs7166271
IL16
15 81307679 intron variant C/T snv 0.12
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11556218
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.030 1.000 3 2011 2013
dbSNP: rs11556218
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.030 1.000 3 2009 2014
dbSNP: rs11556218
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.030 1.000 3 2009 2014
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.030 0.667 3 2015 2019
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.030 0.333 3 2014 2014
dbSNP: rs4778889
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.030 0.333 3 2014 2014
dbSNP: rs7170924
rs7170924
IL16
0.851 0.080 15 81290798 intron variant G/T snv 0.30
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.030 1.000 3 2016 2017
dbSNP: rs1131445
rs1131445
IL16 ; STARD5
0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.020 1.000 2 2008 2014
dbSNP: rs1131445
rs1131445
IL16 ; STARD5
0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 1.000 2 2013 2016
dbSNP: rs1131445
rs1131445
IL16 ; STARD5
0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 1.000 2 2013 2016
dbSNP: rs11556218
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2014 2014
dbSNP: rs11556218
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2014 2014
dbSNP: rs11556218
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.020 0.500 2 2016 2019
dbSNP: rs11556218
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.020 0.500 2 2010 2018
dbSNP: rs4072111
rs4072111
IL16
0.716 0.400 15 81285798 missense variant C/T snv 0.17 0.11
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.020 0.500 2 2016 2018