Variant (rsID / SNP)

rs7103810

rs7103810 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNHD1, RRP8. Location: chromosome 11, position 6,555,365. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DNHD1Not classified

Variant type: missense_variant
Chromosome / position: 11:6555365
HGVS: NM_144666.3,c.2960A>G,p.Asp987Gly
Allele change: Missense_D987G

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.