Variant (rsID / SNP)

rs372108744

rs372108744 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GAL3ST2. Location: chromosome 2, position 242,741,273. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

GAL3ST2Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 2:242741273
Cytoband: 2q37.3
HGVS: NM_022134.3(GAL3ST2):c.197C>T (p.Thr66Met)
Allele change: Missense_T66M

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.