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: rs62209
rs62209
CELF2
1.000 0.080 10 10958376 intron variant G/T snv 0.33
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.800 1.000 1 2011 2011
dbSNP: rs201099
rs201099
CELF2
1.000 0.080 10 10982596 intron variant A/G snv 0.30
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2011 2011
dbSNP: rs201109
rs201109
CELF2
1.000 0.080 10 11000004 intron variant C/T snv 0.31
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2011 2011
dbSNP: rs201119
rs201119
CELF2
1.000 0.080 10 11008014 intron variant T/C snv 0.27
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2011 2011
dbSNP: rs7083575
rs7083575
CELF2 ; CELF2-AS2
10 11080044 intron variant T/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012