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Variant (rsID / SNP)

rs73493606

B3GNT6

rs73493606 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B3GNT6. Location: chromosome 11, position 76,751,166. The table records no clinical significance for this variant.

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Reference-table entries

B3GNT6Not classified
Variant type
missense_variant
Chromosome / position
11:76751166
HGVS
NM_138706.5,c.571G>A,p.Ala191Thr
Allele change
Missense_A191T

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.