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Variant (rsID / SNP)

rs1390938

SLC18A1

rs1390938 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC18A1. Location: chromosome 8, position 20,036,713. The table records no clinical significance for this variant.

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Reference-table entries

SLC18A1Not classified
Variant type
missense_variant
Chromosome / position
8:20036713
HGVS
NM_001135691.3,c.407T>C,p.Ile136Thr
Allele change
Missense_I136T

Associated conditions / phenotypes

Autism|Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome|Autism Spectrum Disorder|Major Affective Disorder 8|Major Affective Disorder 9|Bipolar Disorder|Alcohol Dependence|Mental Depression|Major Depressive Disorder|Depression|Alcohol Use Disorder|Anxiety

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.