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Variant (rsID / SNP)

rs2255317

MATN2

rs2255317 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MATN2. Location: chromosome 8, position 99,044,528. The table records no clinical significance for this variant.

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Reference-table entries

MATN2Not classified
Variant type
missense_variant
Chromosome / position
8:99044528
HGVS
NM_002380.5,c.2564C>T,p.Thr855Met
Allele change
Missense_T814M

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.