Variant (rsID / SNP)

rs4845881

rs4845881 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C1ORF167, C1orf167. Location: chromosome 1, position 11,828,319. The table records no clinical significance for this variant.

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Reference-table entries

C1ORF167Not classified

Variant type: missense_variant
Chromosome / position: 1:11828319
HGVS: NM_001010881.2,c.1529G>A,p.Arg510Gln
Allele change: Missense_R510Q

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.