Variant (rsID / SNP)

rs3762242

rs3762242 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEXMIF. Clinical significance in the table: Benign.

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Reference-table entries

NEXMIFBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq13.3
HGVS: NM_001008537.3(NEXMIF):c.855A>G (p.Leu285=)
Allele change: Synonymous_L285L

Associated conditions / phenotypes

History of neurodevelopmental disorder

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.