Variant (rsID / SNP)

rs1048944

rs1048944 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAI14. Location: chromosome 5, position 34,824,555. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RAI14Not classified

Variant type: missense_variant
Chromosome / position: 5:34824555
HGVS: NM_001145525.2,c.2617G>T,p.Ala873Ser
Allele change: Missense_A841S

Associated conditions / phenotypes

Missense_A862S

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.