Variant (rsID / SNP)

rs367731146

rs367731146 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BSCL2. Location: chromosome 11, position 62,458,748. Clinical significance in the table: Uncertain significance.

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Reference-table entries

BSCL2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 11:62458748
Cytoband: 11q12.3
HGVS: NM_001122955.4(BSCL2):c.1005+4G>A
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.