Variant (rsID / SNP)

rs739134

rs739134 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNU13, C22orf46. Location: chromosome 22, position 42,089,623. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SNU13Not classified

Variant type: upstream_gene_variant
Chromosome / position: 22:42089623
HGVS: NM_001003796.2,c.-4823A>G
Allele change: Missense_W125R

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.