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: rs11191454
rs11191454
AS3MT ; BORCS7-ASMT ; LOC107984265
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.810 1.000 1 2013 2015
dbSNP: rs7085104
rs7085104
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102869116 intron variant A/G snv 0.35
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2013 2019
dbSNP: rs1046778
rs1046778
AS3MT ; BORCS7-ASMT ; LOC107984265
0.851 0.160 10 102901727 3 prime UTR variant T/C snv 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2011 2011
dbSNP: rs11191425
rs11191425
BORCS7-ASMT
1.000 0.040 10 102866213 intron variant C/T snv 1.0E-01
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2009 2009
dbSNP: rs11191447
rs11191447
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102892566 intron variant C/T snv 9.2E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2013 2013
dbSNP: rs12416687
rs12416687
AS3MT ; BORCS7-ASMT
10 102869254 intron variant T/C snv 0.21
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2014 2014
dbSNP: rs4409766
rs4409766
BORCS7 ; BORCS7-ASMT
1.000 0.040 10 102856906 intron variant T/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2009 2009