Source: GWASDB

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: rs3817198
rs3817198
LSP1
0.790 0.280 11 1887776 intron variant T/C snv 0.26
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.800 0.929 2 2007 2017
dbSNP: rs907611
rs907611
LSP1
0.882 0.160 11 1852842 upstream gene variant G/A snv 0.26
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2012 2017
dbSNP: rs907611
rs907611
LSP1
0.882 0.160 11 1852842 upstream gene variant G/A snv 0.26
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.800 1.000 1 2011 2017
dbSNP: rs3817198
rs3817198
LSP1
0.790 0.280 11 1887776 intron variant T/C snv 0.26
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010
dbSNP: rs661348
rs661348
LSP1
11 1884062 intron variant T/C snv 0.43 0.37
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs907611
rs907611
LSP1
0.882 0.160 11 1852842 upstream gene variant G/A snv 0.26
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		0.700 1.000 1 2014 2014