Variant (rsID / SNP)

rs595413

rs595413 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAM217A. Location: chromosome 6, position 4,069,166. The table records no clinical significance for this variant.

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Reference-table entries

FAM217ANot classified

Variant type: missense_variant
Chromosome / position: 6:4069166
HGVS: NM_173563.3,c.1291G>A,p.Val431Ile
Allele change: Missense_V431I

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.