Variant (rsID / SNP)

rs4423040

rs4423040 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FNDC7. Location: chromosome 1, position 109,265,029. The table records no clinical significance for this variant.

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Reference-table entries

FNDC7Not classified

Variant type: missense_variant
Chromosome / position: 1:109265029
HGVS: NM_001144937.3,c.671G>T,p.Arg224Leu
Allele change: Missense_R224L

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.