Variant (rsID / SNP)

rs6986

rs6986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM39-RPP21, RPP21. Location: chromosome 6, position 30,313,340. The table records no clinical significance for this variant.

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Reference-table entries

TRIM39-RPP21Not classified

Variant type: missense_variant
Chromosome / position: 6:30313340
HGVS: NM_001199119.1,c.1278G>C,p.Gln426His
Allele change: Missense_Q426H

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.