Variant (rsID / SNP)

rs62637036

rs62637036 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NYX. The table records no clinical significance for this variant.

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Reference-table entries

NYXNot classified

Variant type: single nucleotide variant
Cytoband: Xp11.4
HGVS: NM_001378477.3(NYX):c.1025T>C (p.Leu342Pro)
Allele change: Missense_L347P

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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