Variant (rsID / SNP)

rs13143848

rs13143848 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C4ORF17, C4orf17. Location: chromosome 4, position 100,443,720. The table records no clinical significance for this variant.

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Reference-table entries

C4ORF17Not classified

Variant type: missense_variant
Chromosome / position: 4:100443720
HGVS: NM_032149.3,c.191G>A,p.Gly64Glu
Allele change: Missense_G64E

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.