Variant (rsID / SNP)

rs371238107

rs371238107 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEF2C. Location: chromosome 5, position 88,119,647. Clinical significance in the table: Benign.

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Reference-table entries

MEF2CBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:88119647
Cytoband: 5q14.3
HGVS: NM_002397.5(MEF2C):c.-42T>C
Allele change: Silent

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.