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: rs3847687
rs3847687
ADGRD1
12 131040508 intron variant C/A;T snv 0.35
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2010 2010
dbSNP: rs11833801
rs11833801
ADGRD1 ; LOC107984452
12 131076849 missense variant G/A;C snv 6.1E-03; 8.0E-06
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11833801
rs11833801
ADGRD1 ; LOC107984452
12 131076849 missense variant G/A;C snv 6.1E-03; 8.0E-06
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1569019
rs1569019
ADGRD1
12 131091646 intron variant C/A;T snv 8.1E-02
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2009 2009
dbSNP: rs1976930
rs1976930
ADGRD1
12 131091900 intron variant C/T snv 9.0E-02
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2009 2009