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Gene entry

FANCM

FA complementation group M

Chromosome
14
Cytoband
14q21.2
Variants (rsID)
29

FANCM is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q21.2). Its official name is “FA complementation group M”. The reference table lists 29 variants (rsID) for this gene.

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Clinically classified variants

23 reference-table entries with clinical significance.

  • rs113986680Benignsingle nucleotide variantFanconi anemia
  • rs1367580Benignsingle nucleotide variantPremature ovarian failure 15|Fanconi anemia|Spermatogenic failure 28
  • rs138151018Benignsingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome
  • rs148675704Benignsingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome
  • rs45547534Benignsingle nucleotide variantFanconi anemia
  • rs45557033Benignsingle nucleotide variantFanconi anemia
  • rs45604036Benignsingle nucleotide variantFanconi anemia
  • rs61746943Benignsingle nucleotide variantFanconi anemia
  • rs61753893Benignsingle nucleotide variantFanconi anemia
  • rs77532752Benignsingle nucleotide variantFanconi anemia
  • rs143006771Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome
  • rs143662421Conflicting interpretationssingle nucleotide variantFanconi anemia|Spermatogenic failure 28|Hereditary cancer-predisposing syndrome
  • rs144567652Conflicting interpretationssingle nucleotide variantFanconi anemia|Spermatogenic failure 28|Malignant germ cell tumor of ovary|Familial cancer of breast|Azoospermia|Hereditary nonpolyposis colorectal carcinoma
  • rs151071546Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome
  • rs200173413Conflicting interpretationssingle nucleotide variantFanconi anemia
  • rs201803784Conflicting interpretationssingle nucleotide variantFanconi anemia|Hereditary breast ovarian cancer syndrome|Hereditary cancer-predisposing syndrome
  • rs77374493Conflicting interpretationssingle nucleotide variantFanconi anemia|Spermatogenic failure 28
  • rs138225703Uncertain significancesingle nucleotide variantFanconi anemia|Spermatogenic failure 28|Premature ovarian failure 15|Spermatogenic failure 28|Hereditary cancer-predisposing syndrome
  • rs139946652Uncertain significancesingle nucleotide variantFanconi anemia|Hereditary cancer-predisposing syndrome
  • rs142747831Uncertain significancesingle nucleotide variantFanconi anemia
  • rs144008013Uncertain significancesingle nucleotide variantFanconi anemia|Fanconi anemia, complementation group M|Spermatogenic failure 28|Premature ovarian failure 15|Spermatogenic failure 28|Hereditary cancer-predisposing syndrome
  • rs146436929Uncertain significancesingle nucleotide variantFanconi anemia
  • rs200717151Uncertain significancesingle nucleotide variantFanconi anemia

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.