Variant (rsID / SNP)

rs7260180

rs7260180 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEACAM20. Location: chromosome 19, position 45,028,169. The table records no clinical significance for this variant.

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Reference-table entries

CEACAM20Not classified

Variant type: missense_variant
Chromosome / position: 19:45028169
HGVS: NM_001102597.3,c.322G>A,p.Val108Ile
Allele change: Missense_V108I

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.