Variant (rsID / SNP)

rs2075761

rs2075761 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGL2. Location: chromosome 7, position 76,828,953. The table records no clinical significance for this variant.

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Reference-table entries

FGL2Not classified

Variant type: missense_variant
Chromosome / position: 7:76828953
HGVS: NM_006682.3,c.158G>A,p.Gly53Glu
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.