Variant (rsID / SNP)

rs9930499

rs9930499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDR42E2. Location: chromosome 16, position 22,192,896. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SDR42E2Not classified

Variant type: missense_variant
Chromosome / position: 16:22192896
HGVS: NM_001365288.2,c.1341G>A,p.Met447Ile

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.