Variant (rsID / SNP)

rs72552273

rs72552273 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC7A7. Location: chromosome 14, position 23,282,625. Clinical significance in the table: Likely benign.

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Reference-table entries

SLC7A7Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 14:23282625
Cytoband: 14q11.2
HGVS: NM_003982.4(SLC7A7):c.-18G>A
Allele change: Silent

Associated conditions / phenotypes

Lysinuric protein intolerance

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.