Variant (rsID / SNP)

rs2295283

rs2295283 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MIIP. Location: chromosome 1, position 12,082,926. The table records no clinical significance for this variant.

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Reference-table entries

MIIPNot classified

Variant type: missense_variant
Chromosome / position: 1:12082926
HGVS: NM_021933.4,c.499A>G,p.Lys167Glu
Allele change: Missense_K167E

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.