Variant (rsID / SNP)

rs734644

rs734644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRL3. Location: chromosome 4, position 62,800,728. The table records no clinical significance for this variant.

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Reference-table entries

ADGRL3Not classified

Variant type: synonymous_variant
Chromosome / position: 4:62800728
HGVS: NM_001387552.1,c.2283T>C,p.Asn761Asn
Allele change: Synonymous_N693N

Associated conditions / phenotypes

Attention Deficit-Hyperactivity Disorder|Major Affective Disorder 8|Major Affective Disorder 9|Bipolar Disorder

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.