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: rs11809810
rs11809810
ACOT11
1 54558033 intron variant A/G snv 6.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17110757
rs17110757
ACOT11
1.000 0.040 1 54584133 intron variant G/A snv 0.20
CUI: C0017638
Disease: Glioma
Glioma 		0.700 1.000 1 2009 2009
dbSNP: rs17110757
rs17110757
ACOT11
1.000 0.040 1 54584133 intron variant G/A snv 0.20
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.700 1.000 1 2009 2009