Variant (rsID / SNP)

rs5569

rs5569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC6A2. Location: chromosome 16, position 55,731,835. Clinical significance in the table: Benign.

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Reference-table entries

SLC6A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:55731835
Cytoband: 16q12.2
HGVS: NM_001172501.3(SLC6A2):c.1287G>A (p.Thr429=)
Allele change: Synonymous_T429T

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.