Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs561077

GPR50

rs561077 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR50. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

GPR50Not classified
Variant type
missense_variant
HGVS
NM_004224.3,c.1594A>G,p.Thr532Ala
Allele change
Missense_T532A

Associated conditions / phenotypes

Scoliosis|Idiopathic Scoliosis|Mental Depression|Major Depressive Disorder|Major Affective Disorder 8|Scoliosis, Isolated 1|Major Affective Disorder 9|Mood Disorder|Bipolar Disorder|Depression

Public references

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