Variant (rsID / SNP)

rs337277

rs337277 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C4ORF33, C4orf33. Location: chromosome 4, position 130,030,652. The table records no clinical significance for this variant.

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Reference-table entries

C4ORF33Not classified

Variant type: missense_variant
Chromosome / position: 4:130030652
HGVS: NM_001099783.2,c.319A>G,p.Met107Val
Allele change: Missense_M107V

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.