Variant (rsID / SNP)

rs1055130

rs1055130 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSCC1. Location: chromosome 8, position 120,847,188. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DSCC1Not classified

Variant type: missense_variant
Chromosome / position: 8:120847188
HGVS: NM_024094.3,c.1127A>G,p.His376Arg
Allele change: Missense_H376R

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.