Variant (rsID / SNP)

rs1128127

rs1128127 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DERL3, SMARCB1. Location: chromosome 22, position 24,179,132. The table records no clinical significance for this variant.

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Reference-table entries

DERL3Not classified

Variant type: missense_variant
Chromosome / position: 22:24179132
HGVS: NM_001002862.3,c.632C>T,p.Ala211Val
Allele change: Missense_A211V

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.