Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs712952

CLTCL1

rs712952 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLTCL1. Location: chromosome 22, position 19,197,949. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

CLTCL1Not classified
Variant type
missense_variant
Chromosome / position
22:19197949
HGVS
NM_007098.4,c.3136C>T,p.Arg1046Cys
Allele change
Missense_R1046C

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.