Variant (rsID / SNP)

rs7207403

rs7207403 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B4GALNT2. Location: chromosome 17, position 47,210,506. The table records no clinical significance for this variant.

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Reference-table entries

B4GALNT2Not classified

Variant type: missense_variant
Chromosome / position: 17:47210506
HGVS: NM_153446.3,c.119C>A,p.Ala40Asp
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.