Variant (rsID / SNP)

rs7602534

rs7602534 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EIF2B4. Location: chromosome 2, position 27,592,423. Clinical significance in the table: Benign.

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Reference-table entries

EIF2B4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:27592423
Cytoband: 2p23.3
HGVS: NM_001034116.2(EIF2B4):c.76-7G>A
Allele change: Silent

Associated conditions / phenotypes

Vanishing white matter disease

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.