Variant (rsID / SNP)

rs115131067

rs115131067 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FANCG. Location: chromosome 9, position 35,078,671. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FANCGBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:35078671
Cytoband: 9p13.3
HGVS: NM_004629.2(FANCG):c.238C>T (p.Leu80=)
Allele change: Synonymous_L80L

Associated conditions / phenotypes

Fanconi anemia|Fanconi anemia complementation group G

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.