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: rs2072803
rs2072803
BTN2A2
1.000 0.040 6 26392287 missense variant G/C snv 8.6E-02 7.7E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2009 2009
dbSNP: rs2072806
rs2072806
BTN2A2
1.000 0.040 6 26384865 intron variant C/G snv 7.7E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2009 2009
dbSNP: rs7756881
rs7756881
BTN2A2
1.000 0.040 6 26389698 intron variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012
dbSNP: rs9461249
rs9461249
BTN2A2
1.000 0.040 6 26383158 5 prime UTR variant T/C snv 0.23
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012