Variant (rsID / SNP)

rs4351475

rs4351475 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM189A2. Location: chromosome 9, position 71,990,645. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FAM189A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:71990645
Cytoband: 9q21.12
HGVS: NM_001347995.2(FAM189A2):c.583-7C>T
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.