Variant (rsID / SNP)

rs763110

rs763110 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FASLG. Location: chromosome 1, position 172,627,498. Clinical significance in the table: risk factor.

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Reference-table entries

FASLGRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 1:172627498
Cytoband: 1q24.3
HGVS: NM_000639.1(FASLG):c.-844C=

Associated conditions / phenotypes

LUNG CANCER, SUSCEPTIBILITY TO

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.