Variant (rsID / SNP)

rs4846833

rs4846833 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALNT2. Location: chromosome 1, position 230,251,823. The table records no clinical significance for this variant.

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Reference-table entries

GALNT2Not classified

Variant type: intron_variant
Chromosome / position: 1:230251823
HGVS: NM_004481.5,c.126+48670G>A
Allele change: Silent

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.