Variant (rsID / SNP)

rs707921

rs707921 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C6ORF47, BAG6, C6orf47. Location: chromosome 6, position 31,625,541. The table records no clinical significance for this variant.

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Reference-table entries

C6ORF47Not classified

Variant type: downstream_gene_variant
Chromosome / position: 6:31625541
HGVS: NM_021184.4,c.*1299G>T
Allele change: Silent

Associated conditions / phenotypes

Pulmonary Disease, Chronic Obstructive|Systemic Lupus Erythematosus|Lupus Erythematosus

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.