Variant (rsID / SNP)

rs1670534

rs1670534 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF212. Location: chromosome 4, position 1,087,265. The table records no clinical significance for this variant.

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Reference-table entries

RNF212Not classified

Variant type: missense_variant
Chromosome / position: 4:1087265
HGVS: NM_001193318.3,c.784A>G,p.Ile262Val
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.