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Variant (rsID / SNP)

rs1060939

MAP1A

rs1060939 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP1A. Location: chromosome 15, position 43,816,917. The table records no clinical significance for this variant.

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Reference-table entries

MAP1ANot classified
Variant type
synonymous_variant
Chromosome / position
15:43816917
HGVS
NM_002373.6,c.3246G>A,p.Gly1082Gly
Allele change
Synonymous_G1082G

Public references

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