Variant (rsID / SNP)

rs2240090

rs2240090 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COBL. Location: chromosome 7, position 51,096,974. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

COBLNot classified

Variant type: missense_variant
Chromosome / position: 7:51096974
HGVS: NM_001287436.3,c.1990G>A,p.Val664Ile
Allele change: Missense_V664I

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.