Variant (rsID / SNP)

rs2164356

rs2164356 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGD5. Location: chromosome 3, position 14,939,479. The table records no clinical significance for this variant.

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Reference-table entries

FGD5Not classified

Variant type: synonymous_variant
Chromosome / position: 3:14939479
HGVS: NM_152536.4,c.2943G>T,p.Leu981Leu
Allele change: Synonymous_L981L

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.