Variant (rsID / SNP)

rs117535770

rs117535770 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2CD3. Location: chromosome 11, position 73,811,643. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

C2CD3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:73811643
Cytoband: 11q13.4
HGVS: NM_001286577.2(C2CD3):c.2659G>A (p.Val887Met)
Allele change: Missense_V887M

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.