Variant (rsID / SNP)

rs4767452

rs4767452 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNFT2. Location: chromosome 12, position 117,217,141. The table records no clinical significance for this variant.

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Reference-table entries

RNFT2Not classified

Variant type: synonymous_variant
Chromosome / position: 12:117217141
HGVS: NM_001109903.2,c.870T>C,p.Ala290Ala
Allele change: Synonymous_A290A

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.