Variant (rsID / SNP)

rs2791494

rs2791494 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLCA1. Location: chromosome 1, position 86,959,173. The table records no clinical significance for this variant.

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Reference-table entries

CLCA1Not classified

Variant type: missense_variant
Chromosome / position: 1:86959173
HGVS: NM_001285.4,c.1571T>C,p.Met524Thr
Allele change: Missense_M524T

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.