Variant (rsID / SNP)

rs243865

rs243865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP2. Location: chromosome 16, position 55,511,806. Clinical significance in the table: association.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MMP2Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 16:55511806
Cytoband: 16q12.2
HGVS: NM_004530.5(MMP2):c.-1586C>T

Associated conditions / phenotypes

Lip and oral cavity carcinoma

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.