Variant (rsID / SNP)

rs1375719

rs1375719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC168. Location: chromosome 13, position 103,410,782. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CCDC168Not classified

Variant type: missense_variant
Chromosome / position: 13:103410782
HGVS: NM_001146197.3,c.286A>G,p.Ile96Val
Allele change: Missense_I96V

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.