Variant (rsID / SNP)

rs1002189

rs1002189 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF215, KIAA1656. Location: chromosome 22, position 30,771,458. The table records no clinical significance for this variant.

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Reference-table entries

RNF215Not classified

Variant type: downstream_gene_variant
Chromosome / position: 22:30771458
HGVS: NM_001017981.2,c.*4131A>G
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.