Variant (rsID / SNP)

rs41271217

rs41271217 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DYNC2I1. Location: chromosome 7, position 158,707,017. Clinical significance in the table: Benign.

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Reference-table entries

DYNC2I1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:158707017
Cytoband: 7q36.3
HGVS: NM_018051.5(DYNC2I1):c.1791+5A>G
Allele change: Silent

Associated conditions / phenotypes

Short-rib thoracic dysplasia 8 with or without polydactyly

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.