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Variant (rsID / SNP)

rs214814

TGM3

rs214814 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGM3. Location: chromosome 20, position 2,297,790. The table records no clinical significance for this variant.

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Reference-table entries

TGM3Not classified
Variant type
missense_variant
Chromosome / position
20:2297790
HGVS
NM_003245.4,c.746G>A,p.Ser249Asn
Allele change
Missense_S249N

Public references

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