Variant (rsID / SNP)

rs111589624

rs111589624 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBM12B. Location: chromosome 8, position 94,747,496. The table records no clinical significance for this variant.

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Reference-table entries

RBM12BNot classified

Variant type: missense_variant
Chromosome / position: 8:94747496
HGVS: NM_001377960.1,c.1143T>G,p.Asp381Glu
Allele change: Missense_D381E

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.