Variant (rsID / SNP)

rs7763726

rs7763726 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FNDC1. Location: chromosome 6, position 159,670,100. The table records no clinical significance for this variant.

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Reference-table entries

FNDC1Not classified

Variant type: missense_variant
Chromosome / position: 6:159670100
HGVS: NM_032532.3,c.4720A>G,p.Thr1574Ala
Allele change: Missense_T1574A

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.