Variant (rsID / SNP)

rs1866374

rs1866374 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP1B. Location: chromosome 5, position 71,490,962. The table records no clinical significance for this variant.

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Reference-table entries

MAP1BNot classified

Variant type: missense_variant
Chromosome / position: 5:71490962
HGVS: NM_005909.5,c.1780A>G,p.Ile594Val
Allele change: Missense_I594V

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.