Variant (rsID / SNP)

rs2544773

rs2544773 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIOK2. Location: chromosome 5, position 96,513,471. The table records no clinical significance for this variant.

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Reference-table entries

RIOK2Not classified

Variant type: missense_variant
Chromosome / position: 5:96513471
HGVS: NM_018343.3,c.287C>G,p.Ser96Cys
Allele change: Missense_S96C

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.