Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs143073792

TACR3

rs143073792 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TACR3. Location: chromosome 4, position 104,510,991. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

TACR3Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
4:104510991
Cytoband
4q24
HGVS
NM_001059.3(TACR3):c.1246A>T (p.Asn416Tyr)
Allele change
Missense_N416Y

Associated conditions / phenotypes

Hypogonadotropic hypogonadism 11 with or without anosmia

Public references

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