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Variant (rsID / SNP)

rs12444859

ADGRG3

rs12444859 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRG3. Location: chromosome 16, position 57,722,328. The table records no clinical significance for this variant.

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Reference-table entries

ADGRG3Not classified
Variant type
synonymous_variant
Chromosome / position
16:57722328
HGVS
NM_170776.5,c.1605C>T,p.Ser535Ser
Allele change
Synonymous_S535S

Public references

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