Variant (rsID / SNP)

rs372532824

rs372532824 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEXN. Location: chromosome 1, position 78,383,674. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NEXNUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:78383674
Cytoband: 1p31.1
HGVS: NM_144573.4(NEXN):c.249G>C (p.Glu83Asp)
Allele change: Synonymous_E83E

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.