Variant (rsID / SNP)

rs11568438

rs11568438 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC7A7. Location: chromosome 14, position 23,282,336. Clinical significance in the table: Benign.

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Reference-table entries

SLC7A7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:23282336
Cytoband: 14q11.2
HGVS: NM_003982.4(SLC7A7):c.272C>T (p.Ala91Val)
Allele change: Missense_A91V

Associated conditions / phenotypes

Lysinuric protein intolerance|Autoinflammatory syndrome

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.