Variant (rsID / SNP)
rs229527
rs229527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C1QTNF6. Location: chromosome 22, position 37,581,485. The table records no clinical significance for this variant.
Reference-table entries
C1QTNF6Not classified
- Variant type
- missense_variant
- Chromosome / position
- 22:37581485
- HGVS
- NM_031910.4,c.62G>T,p.Gly21Val
- Allele change
- Missense_G21V
Associated conditions / phenotypes
Graves' Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.