Variant (rsID / SNP)

rs3808536

rs3808536 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to R3HCC1. Location: chromosome 8, position 23,147,564. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

R3HCC1Not classified

Variant type: splice_acceptor_variant&intron_variant
Chromosome / position: 8:23147564
HGVS: NM_001301650.2,c.309-1G>A
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.