Variant (rsID / SNP)

rs2296978

rs2296978 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B9D1. Location: chromosome 17, position 19,265,952. Clinical significance in the table: Benign.

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Reference-table entries

B9D1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:19265952
Cytoband: 17p11.2
HGVS: NM_015681.6(B9D1):c.-70G>A
Allele change: Silent

Associated conditions / phenotypes

Meckel syndrome, type 9

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.