Variant (rsID / SNP)

rs7972986

rs7972986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GXYLT1. Location: chromosome 12, position 42,481,732. The table records no clinical significance for this variant.

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Reference-table entries

GXYLT1Not classified

Variant type: synonymous_variant
Chromosome / position: 12:42481732
HGVS: NM_173601.2,c.1179C>T,p.Asp393Asp
Allele change: Synonymous_D393D

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.