Variant (rsID / SNP)

rs1042173

rs1042173 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC6A4. Location: chromosome 17, position 28,525,011. Clinical significance in the table: Likely benign.

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Reference-table entries

SLC6A4Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:28525011
Cytoband: 17q11.2
HGVS: NM_001045.6(SLC6A4):c.*463T>G
Allele change: Silent

Associated conditions / phenotypes

Behavior disorder

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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