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: rs10914144
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 4 2009 2014
dbSNP: rs1011731
rs1011731
PIGC ; DNM3
1 172377408 intron variant G/A snv 0.46
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.800 1.000 1 2010 2015
dbSNP: rs10914144
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
dbSNP: rs10914127
rs10914127
DNM3
1 171974808 intron variant A/G snv 0.79
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10914144
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs12075079
rs12075079
DNM3
1 172250855 intron variant A/G snv 0.16
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs17346452
rs17346452
DNM3
1 172084147 intron variant T/C snv 0.19
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs2038479
rs2038479
DNM3
1 171970150 5 prime UTR variant C/A;G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2180748
rs2180748
DNM3
1 171977878 intron variant T/A;G snv
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2014 2014
dbSNP: rs2421992
rs2421992
DNM3
1 172272111 intron variant C/T snv 0.62
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs479336
rs479336
DNM3
1 172230433 intron variant T/A;G snv
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 1 2012 2012
dbSNP: rs678962
rs678962
DNM3
1 172220749 intron variant T/G snv 0.24
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2008 2008