Variant (rsID / SNP)

rs13416004

rs13416004 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NFU1. Location: chromosome 2, position 69,664,976. Clinical significance in the table: Benign.

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Reference-table entries

NFU1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:69664976
Cytoband: 2p13.3
HGVS: NM_001374284.1(NFU1):c.-11+209G>A

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.