Variant (rsID / SNP)

rs2076284

rs2076284 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IYD. Location: chromosome 6, position 150,719,613. Clinical significance in the table: Benign.

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Reference-table entries

IYDBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:150719613
Cytoband: 6q25.1
HGVS: NM_203395.3(IYD):c.*240G>T
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.