Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894845
rs104894845
GLA ; RPL36A-HNRNPH2
0.020 GeneticVariation BEFREE No accumulation of neurologic events in family members of p.A143T patients with stroke/transient ischemic attacks was observed. 27142856

2016
dbSNP: rs104894845
rs104894845
GLA ; RPL36A-HNRNPH2
0.020 GeneticVariation BEFREE The Fabry disease-causing A143T mutation was seen in an African-American male with cryptogenic stroke (0.18% of all strokes: upper 95% CI=0.53%; 0.65% of cryptogenic strokes: upper 95% CI=1.92%). 20007919

2010