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Variant (rsID / SNP)

rs643423

NLRX1

rs643423 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRX1. Location: chromosome 11, position 119,043,656. The table records no clinical significance for this variant.

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Reference-table entries

NLRX1Not classified
Variant type
missense_variant
Chromosome / position
11:119043656
HGVS
NM_001282143.2,c.187C>T,p.Pro63Ser
Allele change
Missense_P63S

Public references

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