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: rs10136789
rs10136789
KCNH5
14 62889535 intron variant T/C snv 0.15
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013
dbSNP: rs10136789
rs10136789
KCNH5
14 62889535 intron variant T/C snv 0.15
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2013 2013
dbSNP: rs4902176
rs4902176
KCNH5
14 62708242 missense variant C/A;G;T snv 8.0E-06; 0.30
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs7143550
rs7143550
KCNH5
14 62740233 intron variant T/C snv 0.55
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011