Source: GWASCAT

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: rs7398375
rs7398375
LRP1 ; LRP1-AS
0.790 0.080 12 57147065 intron variant C/G snv 0.26
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs7398375
rs7398375
LRP1 ; LRP1-AS
0.790 0.080 12 57147065 intron variant C/G snv 0.26
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs7398375
rs7398375
LRP1 ; LRP1-AS
0.790 0.080 12 57147065 intron variant C/G snv 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs11172113
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42
CUI: C0338480
Disease: Common Migraine
Common Migraine 		0.800 1.000 1 2013 2016
dbSNP: rs1466535
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		0.840 1.000 1 2011 2015
dbSNP: rs11172113
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.850 1.000 5 2011 2019