Variant (rsID / SNP)

rs9401790

rs9401790 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF217, RNF217-AS1. Location: chromosome 6, position 125,284,457. The table records no clinical significance for this variant.

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Reference-table entries

RNF217Not classified

Variant type: missense_variant
Chromosome / position: 6:125284457
HGVS: NM_001286398.3,c.767T>C,p.Val256Ala
Allele change: Missense_V256A

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.