Variant (rsID / SNP)

rs771820789

rs771820789 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NF1. Location: chromosome 17, position 29,556,342. Clinical significance in the table: Likely benign.

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Reference-table entries

NF1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:29556342
Cytoband: 17q11.2
HGVS: NM_001042492.3(NF1):c.2709G>T (p.Val903=)
Allele change: Synonymous_V903V

Associated conditions / phenotypes

Neurofibromatosis, type 1

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.