Variant (rsID / SNP)

rs1869609

rs1869609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MATN2. Location: chromosome 8, position 98,991,221. The table records no clinical significance for this variant.

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Reference-table entries

MATN2Not classified

Variant type: missense_variant
Chromosome / position: 8:98991221
HGVS: NM_002380.5,c.1066A>G,p.Lys356Glu
Allele change: Missense_K356E

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.