Variant (rsID / SNP)

rs2250145

rs2250145 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C5ORF46, C5orf46. Location: chromosome 5, position 147,286,054. The table records no clinical significance for this variant.

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Reference-table entries

C5ORF46Not classified

Variant type: missense_variant
Chromosome / position: 5:147286054
HGVS: NM_206966.3,c.11C>T,p.Ser4Leu
Allele change: Missense_S4L

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.