Variant (rsID / SNP)

rs4494160

rs4494160 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FNDC7. Location: chromosome 1, position 109,268,573. The table records no clinical significance for this variant.

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Reference-table entries

FNDC7Not classified

Variant type: missense_variant
Chromosome / position: 1:109268573
HGVS: NM_001144937.3,c.1058T>C,p.Val353Ala
Allele change: Missense_V353A

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.