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Variant (rsID / SNP)

rs1932618

ADGRB3

rs1932618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRB3. Location: chromosome 6, position 69,666,684. The table records no clinical significance for this variant.

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Reference-table entries

ADGRB3Not classified
Variant type
missense_variant
Chromosome / position
6:69666684
HGVS
NM_001704.3,c.1508A>G,p.Asn503Ser
Allele change
Missense_N503S

Public references

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