Variant (rsID / SNP)

rs931196

rs931196 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF830, CCT6B. Location: chromosome 17, position 33,288,882. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZNF830Not classified

Variant type: missense_variant
Chromosome / position: 17:33288882
HGVS: NM_052857.4,c.297T>G,p.His99Gln
Allele change: Missense_H99Q

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.