Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1568923
rs1568923
Entrez Id: 84530
Gene Symbol: SRRM4
SRRM4
CUI: C1863416
Disease:
Autosomal dominant compelling helio ophthalmic outburst syndrome
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016