Variant (rsID / SNP)

rs3745202

rs3745202 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRX. Location: chromosome 19, position 40,901,011. Clinical significance in the table: Benign.

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Reference-table entries

PRXBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:40901011
Cytoband: 19q13.2
HGVS: NM_181882.3(PRX):c.3248C>G (p.Pro1083Arg)
Allele change: Silent

Associated conditions / phenotypes

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