Variant (rsID / SNP)

rs3218613

rs3218613 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAS. Location: chromosome 10, position 90,762,938. Clinical significance in the table: Benign.

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Reference-table entries

FASBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:90762938
Cytoband: 10q23.31
HGVS: NM_000043.6(FAS):c.183G>A (p.Lys61=)
Allele change: Silent

Associated conditions / phenotypes

Autoimmune lymphoproliferative syndrome type 1

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.