Variant (rsID / SNP)

rs186479054

rs186479054 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRG1. Location: chromosome 16, position 57,689,912. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ADGRG1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:57689912
Cytoband: 16q21
HGVS: NM_201525.4(ADGRG1):c.1017+8G>A
Allele change: Silent

Associated conditions / phenotypes

Bilateral frontoparietal polymicrogyria

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.