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: rs10415983
rs10415983
1.000 0.080 19 45208340 intron variant C/T snv 0.26
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2011 2011
dbSNP: rs2159324
rs2159324
19 45192480 intron variant T/C snv 0.36
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2009 2009
dbSNP: rs597668
rs597668
0.925 0.080 19 45205630 intron variant T/A;C;G snv
CUI: C0162534
Disease: Prion Diseases
Prion Diseases
0.700 1.000 1 2012 2012