Variant (rsID / SNP)

rs3130617

rs3130617 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C6ORF47, BAG6, C6orf47. Location: chromosome 6, position 31,627,523. The table records no clinical significance for this variant.

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Reference-table entries

C6ORF47Not classified

Variant type: missense_variant
Chromosome / position: 6:31627523
HGVS: NM_021184.4,c.202G>A,p.Gly68Arg
Allele change: Missense_G68R

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.