Variant (rsID / SNP)

rs12986235

rs12986235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF749. Location: chromosome 19, position 57,955,244. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZNF749Not classified

Variant type: missense_variant
Chromosome / position: 19:57955244
HGVS: NM_001023561.4,c.728A>G,p.Gln243Arg
Allele change: Missense_Q156R

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.