Variant (rsID / SNP)

rs11718898

rs11718898 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAND2. Location: chromosome 3, position 12,848,822. The table records no clinical significance for this variant.

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Reference-table entries

CAND2Not classified

Variant type: missense_variant
Chromosome / position: 3:12848822
HGVS: NM_001162499.2,c.230T>C,p.Val77Ala
Allele change: Missense_V77A

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.