Variant (rsID / SNP)

rs615474

rs615474 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C9ORF131, C9orf131. Location: chromosome 9, position 35,043,291. The table records no clinical significance for this variant.

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Reference-table entries

C9ORF131Not classified

Variant type: missense_variant
Chromosome / position: 9:35043291
HGVS: NM_203299.4,c.665G>T,p.Trp222Leu
Allele change: Missense_W174L

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.