Variant (rsID / SNP)

rs35352238

rs35352238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC105. Location: chromosome 19, position 15,131,330. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CCDC105Not classified

Variant type: missense_variant
Chromosome / position: 19:15131330
HGVS: NM_173482.3,c.733G>A,p.Val245Met
Allele change: Missense_V245M

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.