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: rs10838725
rs10838725
CELF1
0.925 0.160 11 47536319 intron variant T/C snv 0.22
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.820 1.000 1 2013 2018
dbSNP: rs60206633
rs60206633
CELF1
11 47552529 intron variant C/A;G snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs77977823
rs77977823
CELF1
11 47543586 intron variant T/C snv 2.0E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012