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: rs34487851
rs34487851 		0.882 0.200 2 106026098 regulatory region variant A/G snv 0.28
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		0.700 1.000 1 2018 2018
dbSNP: rs35067331
rs35067331
TRAPPC12
1.000 0.120 2 3470314 intron variant C/T snv 0.27
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		0.700 1.000 1 2018 2018
dbSNP: rs429358
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		0.700 1.000 1 2018 2018
dbSNP: rs6857
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		0.700 1.000 1 2014 2014
dbSNP: rs79524815
rs79524815
HDAC9
0.851 0.240 7 18658708 intron variant T/G snv 3.8E-02
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
Cerebral Amyloid Angiopathy 		0.700 1.000 1 2018 2018