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Variant (rsID / SNP)

rs145574885

MED25

rs145574885 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MED25. Location: chromosome 19, position 50,331,754. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MED25Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
19:50331754
Cytoband
19q13.33
HGVS
NM_030973.4(MED25):c.354C>T (p.Leu118=)
Allele change
Synonymous_L118L

Associated conditions / phenotypes

Charcot-Marie-Tooth disease type 2|Charcot-Marie-Tooth disease

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.