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: rs11847697
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 2 2010 2013
dbSNP: rs11847697
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 2 2010 2013
dbSNP: rs12589992
rs12589992
PRKD1
14 29918314 intron variant C/T snv 6.9E-02
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2012 2012