Variant (rsID / SNP)

rs3733631

rs3733631 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TACR3. Location: chromosome 4, position 104,641,103. Clinical significance in the table: Benign.

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Reference-table entries

TACR3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:104641103
Cytoband: 4q24
HGVS: NM_001059.3(TACR3):c.-271C>G

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.