Variant (rsID / SNP)
rs3130062
rs3130062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NFKBIL1. Location: chromosome 6, position 31,525,912. The table records no clinical significance for this variant.
Reference-table entries
NFKBIL1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:31525912
- HGVS
- NM_005007.4,c.670C>T,p.Arg224Cys
- Allele change
- Missense_R186C
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.