Variant (rsID / SNP)

rs3751821

rs3751821 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCP110. Location: chromosome 16, position 19,547,503. Clinical significance in the table: Benign.

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Reference-table entries

CCP110Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:19547503
Cytoband: 16p12.3
HGVS: NM_001323572.2(CCP110):c.512C>T (p.Pro171Leu)
Allele change: Missense_P171L

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.