Variant (rsID / SNP)

rs17860299

rs17860299 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CELA1. Location: chromosome 12, position 51,737,607. The table records no clinical significance for this variant.

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Reference-table entries

CELA1Not classified

Variant type: missense_variant
Chromosome / position: 12:51737607
HGVS: NM_001971.6,c.130C>T,p.Arg44Trp
Allele change: Missense_R44W

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.