Variant (rsID / SNP)

rs145477274

rs145477274 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAN1B1. Location: chromosome 9, position 139,996,099. Clinical significance in the table: Benign.

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Reference-table entries

MAN1B1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:139996099
Cytoband: 9q34.3
HGVS: NM_016219.5(MAN1B1):c.1229G>A (p.Arg410His)
Allele change: Missense_R410H

Associated conditions / phenotypes

History of neurodevelopmental disorder|Rafiq syndrome

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.