Variant (rsID / SNP)

rs7076888

rs7076888 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SORBS1. Location: chromosome 10, position 97,116,219. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SORBS1Not classified

Variant type: synonymous_variant
Chromosome / position: 10:97116219
HGVS: NM_001384452.1,c.2169G>A,p.Leu723Leu
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.