Variant (rsID / SNP)

rs148028531

rs148028531 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBM28. Location: chromosome 7, position 127,950,857. Clinical significance in the table: Benign.

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Reference-table entries

RBM28Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:127950857
Cytoband: 7q32.1
HGVS: NM_018077.3(RBM28):c.2273A>G (p.Asp758Gly)
Allele change: Missense_D758G

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.