Variant (rsID / SNP)

rs2187094

rs2187094 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC102B. Location: chromosome 18, position 66,513,615. The table records no clinical significance for this variant.

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Reference-table entries

CCDC102BNot classified

Variant type: missense_variant
Chromosome / position: 18:66513615
HGVS: NM_001093729.2,c.893A>G,p.Lys298Arg
Allele change: Missense_K298R

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.