Variant (rsID / SNP)

rs145976466

rs145976466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RTTN. Location: chromosome 18, position 67,687,966. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RTTNBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:67687966
Cytoband: 18q22.2
HGVS: NM_173630.4(RTTN):c.6038G>T (p.Cys2013Phe)
Allele change: Missense_C1101F

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.