Variant (rsID / SNP)

rs1126618

rs1126618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C4BPA. Location: chromosome 1, position 207,297,680. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

C4BPABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:207297680
Cytoband: 1q32.2
HGVS: NM_000715.4(C4BPA):c.675T>C (p.Gly225=)
Allele change: Synonymous_G225G

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.