Variant (rsID / SNP)

rs373177231

rs373177231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MBD5. Location: chromosome 2, position 149,247,255. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MBD5Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 2:149247255
Cytoband: 2q23.1
HGVS: NM_001378120.1(MBD5):c.4054G>T (p.Ala1352Ser)
Allele change: Missense_A1119S

Associated conditions / phenotypes

Intellectual disability, autosomal dominant 1

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.