rs13107325 associated_with SLC39A8
Evidence from:
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Evidence (3 sources)
Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals.
(2023)
PMID:38062264
cited
five missense variants (... SCL39A8*rs13107325 ...)
confidence: 0.95
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
(2022)
PMID:35396580
cited
SLC39A8 in which rs13107325 ... is now strongly supported as causal (PP > 0.99).
confidence: 0.96
Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts.
(2019)
PMID:30336701
cited
The exonic SNPs (rs601338, rs17651549, rs13107325) of FUT2, MAPT and SLC39A8, respectively, had the highest CADD scores (>34)
confidence: 0.95