Variant (rsID / SNP)

rs10797347

rs10797347 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP104. Location: chromosome 1, position 3,759,784. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CEP104Not classified

Variant type: intron_variant
Chromosome / position: 1:3759784
HGVS: NM_014704.4,c.566+1687T>C
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.