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Variant (rsID / SNP)

rs199476043

NLRX1

rs199476043 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRX1. Location: chromosome 11, position 119,045,226. The table records no clinical significance for this variant.

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Reference-table entries

NLRX1Not classified
Variant type
single nucleotide variant
Chromosome / position
11:119045226
Cytoband
11q23.3
HGVS
NM_001282144.2(NLRX1):c.914G>A (p.Arg305His)
Allele change
Missense_R305H

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.