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Variant (rsID / SNP)

rs180177196

AGXT

rs180177196 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGXT. Location: chromosome 2, position 241,808,729. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

AGXTOther
Clinical significance (as recorded)
no interpretation for the single variant
Variant type
single nucleotide variant
Chromosome / position
2:241808729
Cytoband
2q37.3
HGVS
NM_000030.3(AGXT):c.308G>A (p.Gly103Glu)
Allele change
Missense_G103E

Public references

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