Variant (rsID / SNP)

rs5998267

rs5998267 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C22ORF42, C22orf42. Location: chromosome 22, position 32,554,985. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

C22ORF42Not classified

Variant type: missense_variant
Chromosome / position: 22:32554985
HGVS: NM_001010859.3,c.218T>C,p.Leu73Pro
Allele change: Missense_L73P

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.