Variant (rsID / SNP)

rs80358237

rs80358237 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FASLG. Location: chromosome 1, position 172,635,050. The table records no clinical significance for this variant.

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Reference-table entries

FASLGNot classified

Variant type: single nucleotide variant
Chromosome / position: 1:172635050
Cytoband: 1q24.3
HGVS: NM_000639.3(FASLG):c.740C>A (p.Ala247Glu)
Allele change: Missense_A247E

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.