Variant (rsID / SNP)

rs142338628

rs142338628 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP2. Location: chromosome 2, position 210,559,148. Clinical significance in the table: Uncertain significance.

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Reference-table entries

MAP2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:210559148
Cytoband: 2q34
HGVS: NM_001375505.1(MAP2):c.2254G>T (p.Ala752Ser)
Allele change: Missense_A748S

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.