Variant (rsID / SNP)

rs12956068

rs12956068 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RTTN. Location: chromosome 18, position 67,864,918. Clinical significance in the table: Likely benign.

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Reference-table entries

RTTNLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 18:67864918
Cytoband: 18q22.2
HGVS: NM_173630.4(RTTN):c.635A>C (p.Asp212Ala)
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.