Variant (rsID / SNP)

rs2249769

rs2249769 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZSCAN30, ZNF397. Location: chromosome 18, position 32,834,186. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZSCAN30Not classified

Variant type: missense_variant
Chromosome / position: 18:32834186
HGVS: NM_001112734.4,c.713A>C,p.Gln238Pro
Allele change: Silent

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.