Variant (rsID / SNP)

rs12912505

rs12912505 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP1A. Location: chromosome 15, position 43,817,404. The table records no clinical significance for this variant.

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Reference-table entries

MAP1ANot classified

Variant type: missense_variant
Chromosome / position: 15:43817404
HGVS: NM_002373.6,c.3733G>A,p.Asp1245Asn
Allele change: Missense_D1245N

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.