Variant (rsID / SNP)

rs201635818

rs201635818 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRID2. Location: chromosome 4, position 94,137,998. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GRID2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 4:94137998
Cytoband: 4q22.2
HGVS: NM_001510.4(GRID2):c.899G>A (p.Arg300His)
Allele change: Missense_R205H

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.