Variant (rsID / SNP)

rs2168101

rs2168101 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMO1. Location: chromosome 11, position 8,255,408. Clinical significance in the table: Benign.

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Reference-table entries

LMO1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:8255408
Cytoband: 11p15.4
HGVS: NM_002315.3(LMO1):c.26-3357G>T
Allele change: Silent

Associated conditions / phenotypes

LIM DOMAIN ONLY-1 POLYMORPHISM

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.