Variant (rsID / SNP)

rs6005977

rs6005977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C22ORF31, C22orf31. Location: chromosome 22, position 29,456,733. The table records no clinical significance for this variant.

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Reference-table entries

C22ORF31Not classified

Variant type: synonymous_variant
Chromosome / position: 22:29456733
HGVS: NM_015370.2,c.102A>G,p.Ser34Ser
Allele change: Synonymous_S34S

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.