Variant (rsID / SNP)

rs6835769

rs6835769 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FRAS1. Location: chromosome 4, position 79,284,694. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FRAS1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:79284694
Cytoband: 4q21.21
HGVS: NM_025074.7(FRAS1):c.2450C>T (p.Ala817Val)
Allele change: Missense_A817V

Associated conditions / phenotypes

Fraser syndrome 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.