Variant (rsID / SNP)

rs183860695

rs183860695 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEACAM16. Location: chromosome 19, position 45,206,933. Clinical significance in the table: Benign.

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Reference-table entries

CEACAM16Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:45206933
Cytoband: 19q13.32
HGVS: NM_001039213.4(CEACAM16):c.352G>A (p.Glu118Lys)
Allele change: Missense_E118K

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.