Variant (rsID / SNP)

rs386360

rs386360 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FNDC1. Location: chromosome 6, position 159,660,879. The table records no clinical significance for this variant.

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Reference-table entries

FNDC1Not classified

Variant type: missense_variant
Chromosome / position: 6:159660879
HGVS: NM_032532.3,c.4511C>A,p.Thr1504Lys
Allele change: Missense_T1504K

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.