Variant (rsID / SNP)

rs10120210

rs10120210 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ECM2. Location: chromosome 9, position 95,284,982. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ECM2Not classified

Variant type: missense_variant
Chromosome / position: 9:95284982
HGVS: NM_001393.4,c.167A>C,p.Gln56Pro
Allele change: Silent

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.