Variant (rsID / SNP)

rs3733632

rs3733632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TACR3. Location: chromosome 4, position 104,640,935. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TACR3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:104640935
Cytoband: 4q24
HGVS: NM_001059.3(TACR3):c.-103T>C
Allele change: Silent

Associated conditions / phenotypes

Hypogonadotropic hypogonadism 11 with or without anosmia

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.