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Variant (rsID / SNP)

rs112775979

ADGRG1

rs112775979 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRG1. Location: chromosome 16, position 57,684,189. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ADGRG1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:57684189
Cytoband
16q21
HGVS
NM_201525.4(ADGRG1):c.-11G>A
Allele change
Silent

Associated conditions / phenotypes

Bilateral frontoparietal polymicrogyria

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.