Variant (rsID / SNP)

rs1533594

rs1533594 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RTP4. Location: chromosome 3, position 187,088,926. The table records no clinical significance for this variant.

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Reference-table entries

RTP4Not classified

Variant type: missense_variant
Chromosome / position: 3:187088926
HGVS: NM_022147.3,c.506G>A,p.Cys169Tyr
Allele change: Missense_C169Y

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.