Variant (rsID / SNP)
rs1046668
rs1046668 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFAIP6. Location: chromosome 2, position 152,226,570. The table records no clinical significance for this variant.
Reference-table entries
TNFAIP6Not classified
- Variant type
- missense_variant
- Chromosome / position
- 2:152226570
- HGVS
- NM_007115.4,c.431A>G,p.Gln144Arg
- Allele change
- Silent
Associated conditions / phenotypes
Autoimmune Disease|Multiple Sclerosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.