Variant (rsID / SNP)

rs11808092

rs11808092 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EVI5. Location: chromosome 1, position 93,073,228. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

EVI5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:93073228
Cytoband: 1p22.1
HGVS: NM_001350197.2(EVI5):c.1884G>T (p.Gln628His)
Allele change: Missense_Q628H

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.