Variant (rsID / SNP)

rs35140809

rs35140809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AFDN. Location: chromosome 6, position 168,297,647. Clinical significance in the table: Uncertain significance.

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Reference-table entries

AFDNUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:168297647
Cytoband: 6q27
HGVS: NM_001386888.1(AFDN):c.1312A>G (p.Ile438Val)
Allele change: Missense_I422V

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.