Variant (rsID / SNP)

rs371138642

rs371138642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GDAP1. Location: chromosome 8, position 75,263,639. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GDAP1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 8:75263639
Cytoband: 8q21.11
HGVS: NM_018972.4(GDAP1):c.248G>C (p.Gly83Ala)
Allele change: Silent

Associated conditions / phenotypes

Charcot-Marie-Tooth disease type 4A|Charcot-Marie-Tooth 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.