Variant (rsID / SNP)

rs248248

rs248248 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRNIP. Location: chromosome 5, position 179,267,949. The table records no clinical significance for this variant.

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Reference-table entries

MRNIPNot classified

Variant type: missense_variant
Chromosome / position: 5:179267949
HGVS: NM_016175.4,c.460A>G,p.Arg154Gly
Allele change: Missense_R99G

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.