Variant (rsID / SNP)

rs61749868

rs61749868 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF135. Location: chromosome 17, position 29,326,155. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RNF135Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:29326155
Cytoband: 17q11.2
HGVS: NM_032322.4(RNF135):c.1245G>T (p.Trp415Cys)
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.