Variant (rsID / SNP)

rs2075465

rs2075465 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROGDI, SMIM22. Location: chromosome 16, position 4,846,068. The table records no clinical significance for this variant.

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Reference-table entries

ROGDINot classified

Variant type: downstream_gene_variant
Chromosome / position: 16:4846068
HGVS: NM_024589.3,c.*1393A>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.