Variant (rsID / SNP)

rs17281188

rs17281188 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC38A5. Clinical significance in the table: Benign.

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Reference-table entries

SLC38A5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp11.23
HGVS: NM_033518.4(SLC38A5):c.1352T>C (p.Met451Thr)
Allele change: Missense_M451T

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.