Variant (rsID / SNP)

rs2072490

rs2072490 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAST3. Location: chromosome 19, position 18,257,750. The table records no clinical significance for this variant.

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Reference-table entries

MAST3Not classified

Variant type: synonymous_variant
Chromosome / position: 19:18257750
HGVS: NM_001393501.1,c.3246C>T,p.Gly1082Gly
Allele change: Synonymous_G1045G

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.