Variant (rsID / SNP)

rs2811795

rs2811795 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC183, RABL6. Location: chromosome 9, position 139,700,605. The table records no clinical significance for this variant.

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Reference-table entries

CCDC183Not classified

Variant type: missense_variant
Chromosome / position: 9:139700605
HGVS: NM_001039374.5,c.1024T>C,p.Trp342Arg
Allele change: Missense_W342R

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.