Variant (rsID / SNP)

rs278981

rs278981 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBM47. Location: chromosome 4, position 40,428,010. The table records no clinical significance for this variant.

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Reference-table entries

RBM47Not classified

Variant type: missense_variant
Chromosome / position: 4:40428010
HGVS: NM_001098634.2,c.1693A>G,p.Met565Val
Allele change: Missense_M565V

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.