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: rs17118552
rs17118552
MDGA2
1.000 0.120 14 47405354 intron variant A/G snv 5.6E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 1 2013 2013
dbSNP: rs11627056
rs11627056
MDGA2
14 46985783 intron variant G/A snv 0.29
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs12883384
rs12883384
MDGA2
1.000 0.040 14 46934481 intron variant A/C;T snv
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM 		0.700 1.000 1 2008 2008
dbSNP: rs1955811
rs1955811
MDGA2
1.000 0.080 14 47535397 intron variant A/T snv 0.75
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs3007103
rs3007103
MDGA2
14 46897137 intron variant A/G snv 0.58
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs7159841
rs7159841
MDGA2
14 47394632 intron variant C/T snv 0.72
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2007 2007
dbSNP: rs7159841
rs7159841
MDGA2
14 47394632 intron variant C/T snv 0.72
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2007 2007