Variant (rsID / SNP)

rs138275098

rs138275098 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAT4. Location: chromosome 4, position 126,373,858. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FAT4Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:126373858
Cytoband: 4q28.1
HGVS: NM_001291303.3(FAT4):c.11693C>T (p.Ala3898Val)
Allele change: Missense_A3896V

Associated conditions / phenotypes

7 conditions

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.