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Variant (rsID / SNP)

rs2145412

CLCA1

rs2145412 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLCA1. Location: chromosome 1, position 86,939,130. The table records no clinical significance for this variant.

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Reference-table entries

CLCA1Not classified
Variant type
missense_variant
Chromosome / position
1:86939130
HGVS
NM_001285.4,c.193C>T,p.Leu65Phe
Allele change
Missense_L65F

Public references

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