Variant (rsID / SNP)

rs16837960

rs16837960 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C4ORF50, C4orf50. Location: chromosome 4, position 5,975,538. The table records no clinical significance for this variant.

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Reference-table entries

C4ORF50Not classified

Variant type: missense_variant
Chromosome / position: 4:5975538
HGVS: NM_001364689.2,c.3952C>T,p.Arg1318Trp
Allele change: Missense_R1139W

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.