Variant (rsID / SNP)

rs10935070

rs10935070 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TOPBP1. Location: chromosome 3, position 133,341,988. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TOPBP1Not classified

Variant type: missense_variant
Chromosome / position: 3:133341988
HGVS: NM_007027.4,c.3125A>G,p.Asn1042Ser
Allele change: Missense_N1042S

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.