Source: GWASCAT

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: rs12897422
rs12897422
AP1G2 ; LOC102724814
14 23563818 missense variant G/A;C;T snv 9.6E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2281680
rs2281680
AP1G2 ; LOC102724814
14 23563861 splice region variant C/T snv 0.18 0.13
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death 		0.700 1.000 1 2011 2011
dbSNP: rs77436356
rs77436356
AP1G2 ; LOC102724814
14 23565807 non coding transcript exon variant C/T snv 6.2E-03 6.0E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019