Variant (rsID / SNP)

rs11722554

rs11722554 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYTL1. Location: chromosome 4, position 5,016,883. The table records no clinical significance for this variant.

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Reference-table entries

CYTL1Not classified

Variant type: missense_variant
Chromosome / position: 4:5016883
HGVS: NM_018659.3,c.406C>T,p.Arg136Cys
Allele change: Missense_R136C

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.