Variant (rsID / SNP)

rs2388982

rs2388982 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RESF1. Location: chromosome 12, position 32,134,240. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RESF1Not classified

Variant type: synonymous_variant
Chromosome / position: 12:32134240
HGVS: NM_018169.4,c.351C>T,p.Asn117Asn
Allele change: Synonymous_N117N

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.