Variant (rsID / SNP)
rs4245191
rs4245191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRX1. Location: chromosome 11, position 119,052,826. The table records no clinical significance for this variant.
Reference-table entries
NLRX1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:119052826
- HGVS
- NM_001282143.2,c.2378C>A,p.Ala793Glu
- Allele change
- Missense_A793E
Associated conditions / phenotypes
Type 2 Diabetes Mellitus|Diabetes Mellitus
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.