Variant (rsID / SNP)

rs1055055

rs1055055 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIMKLA. Location: chromosome 1, position 42,880,516. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RIMKLANot classified

Variant type: synonymous_variant
Chromosome / position: 1:42880516
HGVS: NM_173642.4,c.1047T>C,p.Ser349Ser
Allele change: Synonymous_S349S

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.