Variant (rsID / SNP)

rs3749988

rs3749988 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XG. The table records no clinical significance for this variant.

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Reference-table entries

XGNot classified

Variant type: missense_variant
HGVS: NM_001141919.2,c.392T>C,p.Leu131Pro
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.