Variant (rsID / SNP)

rs1014867

rs1014867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT4. Location: chromosome 4, position 126,412,891. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FAT4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:126412891
Cytoband: 4q28.1
HGVS: NM_001291303.3(FAT4):c.14920C>T (p.Pro4974Ser)
Allele change: Missense_P4972S

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.