Variant (rsID / SNP)

rs1367580

rs1367580 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCM. Location: chromosome 14, position 45,644,589. Clinical significance in the table: Benign.

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Reference-table entries

FANCMBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:45644589
Cytoband: 14q21.2
HGVS: NM_020937.4(FANCM):c.2632G>T (p.Val878Leu)
Allele change: Missense_V852L

Associated conditions / phenotypes

Premature ovarian failure 15|Fanconi anemia|Spermatogenic failure 28

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.