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Variant (rsID / SNP)

rs1061325

CLTCL1

rs1061325 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLTCL1. Location: chromosome 22, position 19,184,095. The table records no clinical significance for this variant.

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Reference-table entries

CLTCL1Not classified
Variant type
missense_variant
Chromosome / position
22:19184095
HGVS
NM_007098.4,c.3946A>G,p.Met1316Val
Allele change
Missense_M1316V

Public references

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