Variant (rsID / SNP)

rs34925488

rs34925488 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LACTB. Location: chromosome 15, position 63,414,116. Clinical significance in the table: Benign.

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Reference-table entries

LACTBBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:63414116
Cytoband: 15q22.2
HGVS: NM_032857.5(LACTB):c.46G>C (p.Gly16Arg)
Allele change: Missense_G16R

Associated conditions / phenotypes

Abnormality of neuronal migration

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.