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: rs1132896
rs1132896
16 55485623 synonymous variant G/C snv 0.31 0.26
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2018 2018
dbSNP: rs243832
rs243832
16 55505279 intron variant C/G snv 0.50
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 < 0.001 1 2018 2018
dbSNP: rs7201
rs7201
0.925 0.160 16 55505702 3 prime UTR variant A/C snv 0.37
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 < 0.001 1 2018 2018