Variant (rsID / SNP)

rs1339374

rs1339374 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC107, ARHGEF39. Location: chromosome 9, position 35,660,990. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CCDC107Not classified

Variant type: missense_variant
Chromosome / position: 9:35660990
HGVS: NM_174923.3,c.658A>G,p.Ile220Val
Allele change: Silent

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.