Variant (rsID / SNP)

rs35351680

rs35351680 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MATK. Location: chromosome 19, position 3,778,219. The table records no clinical significance for this variant.

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Reference-table entries

MATKNot classified

Variant type: missense_variant
Chromosome / position: 19:3778219
HGVS: NM_002378.4,c.1489G>A,p.Ala497Thr
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.