Variant (rsID / SNP)

rs73991652

rs73991652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C2CD6. Location: chromosome 2, position 202,430,584. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

C2CD6Not classified

Variant type: missense_variant
Chromosome / position: 2:202430584
HGVS: NM_001168221.2,c.845C>T,p.Thr282Ile
Allele change: Missense_T282I

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.