Variant (rsID / SNP)

rs201182031

rs201182031 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRID1. Location: chromosome 10, position 87,966,199. Clinical significance in the table: Benign.

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Reference-table entries

GRID1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:87966199
Cytoband: 10q23.2
HGVS: NM_017551.3(GRID1):c.442C>T (p.Arg148Cys)
Allele change: Missense_R148C

Associated conditions / phenotypes

Abnormality of neuronal migration

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.