Variant (rsID / SNP)

rs17037858

rs17037858 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C4ORF45, C4orf45. Location: chromosome 4, position 159,894,277. The table records no clinical significance for this variant.

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Reference-table entries

C4ORF45Not classified

Variant type: missense_variant
Chromosome / position: 4:159894277
HGVS: NM_152543.3,c.251A>G,p.Tyr84Cys
Allele change: Missense_Y84C

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.