Variant (rsID / SNP)

rs1633399

rs1633399 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLTCL1. Location: chromosome 22, position 19,183,787. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CLTCL1Not classified

Variant type: missense_variant
Chromosome / position: 22:19183787
HGVS: NM_007098.4,c.4181T>C,p.Ile1394Thr
Allele change: Missense_I1394T

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.