Variant (rsID / SNP)

rs10036156

rs10036156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GABRP. Location: chromosome 5, position 170,215,638. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

GABRPNot classified

Variant type: synonymous_variant
Chromosome / position: 5:170215638
HGVS: NM_014211.3,c.19T>C,p.Leu7Leu
Allele change: Synonymous_L7L

Associated conditions / phenotypes

Mental Depression|Major Depressive Disorder|Depression

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.