Variant (rsID / SNP)

rs2235076

rs2235076 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRIK2. Location: chromosome 6, position 102,516,260. Clinical significance in the table: Benign.

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Reference-table entries

GRIK2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:102516260
Cytoband: 6q16.3
HGVS: NM_021956.5(GRIK2):c.2601G>A (p.Met867Ile)
Allele change: Silent

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.