Variant (rsID / SNP)

rs36092077

rs36092077 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HTR3D. Location: chromosome 3, position 183,753,777. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

HTR3DNot classified

Variant type: missense_variant
Chromosome / position: 3:183753777
HGVS: NM_001163646.2,c.269G>A,p.Arg90Gln
Allele change: Silent

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.