Variant (rsID / SNP)

rs160632

rs160632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIOK2. Location: chromosome 5, position 96,503,523. The table records no clinical significance for this variant.

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Reference-table entries

RIOK2Not classified

Variant type: missense_variant
Chromosome / position: 5:96503523
HGVS: NM_018343.3,c.1045G>A,p.Gly349Arg
Allele change: Missense_G349R

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.