Variant (rsID / SNP)

rs2032887

rs2032887 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCL25. Location: chromosome 19, position 8,121,360. The table records no clinical significance for this variant.

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Reference-table entries

CCL25Not classified

Variant type: missense_variant
Chromosome / position: 19:8121360
HGVS: NM_001394634.1,c.302A>G,p.His101Arg
Allele change: Missense_H101R

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.