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Variant (rsID / SNP)

rs2307046

RBM47

rs2307046 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RBM47. Location: chromosome 4, position 40,438,576. The table records no clinical significance for this variant.

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Reference-table entries

RBM47Not classified
Variant type
synonymous_variant
Chromosome / position
4:40438576
HGVS
NM_001098634.2,c.1212T>C,p.Gly404Gly
Allele change
Synonymous_G404G

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.