Variant (rsID / SNP)

rs117843366

rs117843366 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RTTN. Location: chromosome 18, position 67,817,837. Clinical significance in the table: Benign.

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Reference-table entries

RTTNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:67817837
Cytoband: 18q22.2
HGVS: NM_173630.4(RTTN):c.2055+7C>T
Allele change: Silent

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.