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Gene entry

FRAS1

Fraser extracellular matrix complex subunit 1

Chromosome
4
Cytoband
4q21.21
Variants (rsID)
132

FRAS1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q21.21). Its official name is “Fraser extracellular matrix complex subunit 1”. The reference table lists 132 variants (rsID) for this gene.

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Clinically classified variants

29 reference-table entries with clinical significance.

  • rs114077522Benignsingle nucleotide variantFraser syndrome 1
  • rs114190041Benignsingle nucleotide variantFraser syndrome 1
  • rs12504081Benignsingle nucleotide variantFraser syndrome 1
  • rs142389362Benignsingle nucleotide variantFraser syndrome 1
  • rs144715071Benignsingle nucleotide variantFraser syndrome 1
  • rs145035489Benignsingle nucleotide variantFraser syndrome 1
  • rs147332320Benignsingle nucleotide variantFraser syndrome 1
  • rs151307846Benignsingle nucleotide variantFraser syndrome 1
  • rs17003071Benignsingle nucleotide variantFraser syndrome 1
  • rs17459809Benignsingle nucleotide variantFraser syndrome 1
  • rs199921300Benignsingle nucleotide variantFraser syndrome 1
  • rs34237418Benignsingle nucleotide variantFraser syndrome 1
  • rs345513Benignsingle nucleotide variantFraser syndrome 1
  • rs61729366Benignsingle nucleotide variantFraser syndrome 1|Congenital diaphragmatic hernia
  • rs6835769Benignsingle nucleotide variantFraser syndrome 1
  • rs7699637Benignsingle nucleotide variantFraser syndrome 1
  • rs140492803Conflicting interpretationssingle nucleotide variantFraser syndrome 1
  • rs144530996Conflicting interpretationssingle nucleotide variantFraser syndrome 1
  • rs148663672Conflicting interpretationssingle nucleotide variantFraser syndrome 1
  • rs17003166Conflicting interpretationssingle nucleotide variantFraser syndrome 1
  • rs1872267Conflicting interpretationssingle nucleotide variantFraser syndrome 1
  • rs189612722Conflicting interpretationssingle nucleotide variant
  • rs200346497Conflicting interpretationssingle nucleotide variantAnophthalmia-microphthalmia syndrome|Fraser syndrome 1
  • rs35219594Conflicting interpretationssingle nucleotide variantFraser syndrome 1
  • rs745597204Conflicting interpretationssingle nucleotide variantFraser syndrome 1|Congenital anomaly of kidney and urinary tract
  • rs192225415Likely benignsingle nucleotide variantFraser syndrome 1
  • rs377046630Pathogenicsingle nucleotide variantFraser syndrome 1
  • rs150567662Uncertain significancesingle nucleotide variant
  • rs186811333Uncertain significancesingle nucleotide variantFraser syndrome 1

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.