Variant (rsID / SNP)

rs2234767

rs2234767 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAS, ACTA2. Location: chromosome 10, position 90,749,256. Clinical significance in the table: risk factor.

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Reference-table entries

FASRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 10:90749256
Cytoband: 10q23.31
HGVS: NM_001141945.2(ACTA2):c.-24+1440C>T
Allele change: Silent

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.