Variant (rsID / SNP)

rs150567662

rs150567662 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FRAS1. Location: chromosome 4, position 79,460,466. Clinical significance in the table: Uncertain significance.

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Reference-table entries

FRAS1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 4:79460466
Cytoband: 4q21.21
HGVS: NM_025074.7(FRAS1):c.11317G>C (p.Val3773Leu)
Allele change: Missense_V3773L

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.