Variant (rsID / SNP)

rs1491242

rs1491242 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C4ORF54, C4orf54. Location: chromosome 4, position 100,571,001. The table records no clinical significance for this variant.

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Reference-table entries

C4ORF54Not classified

Variant type: missense_variant
Chromosome / position: 4:100571001
HGVS: NM_001354435.2,c.4805A>G,p.Gln1602Arg
Allele change: Missense_Q1602R

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.