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Variant (rsID / SNP)

rs2072788

MATN4

rs2072788 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MATN4. Location: chromosome 20, position 43,933,021. The table records no clinical significance for this variant.

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Reference-table entries

MATN4Not classified
Variant type
missense_variant
Chromosome / position
20:43933021
HGVS
NM_001393530.1,c.490C>A,p.Arg164Ser
Allele change
Missense_R164S

Public references

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