Variant (rsID / SNP)

rs1337677

rs1337677 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRIN3A. Location: chromosome 9, position 104,499,575. The table records no clinical significance for this variant.

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Reference-table entries

GRIN3ANot classified

Variant type: synonymous_variant
Chromosome / position: 9:104499575
HGVS: NM_133445.3,c.687A>G,p.Pro229Pro
Allele change: Synonymous_P229P

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.