Variant (rsID / SNP)
rs1798192
rs1798192 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HCAR3. Location: chromosome 12, position 123,200,768. The table records no clinical significance for this variant.
Reference-table entries
HCAR3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:123200768
- HGVS
- NM_006018.3,c.517A>C,p.Thr173Pro
- Allele change
- Missense_T173P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.