Variant (rsID / SNP)

rs73947814

rs73947814 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALMS1. Location: chromosome 2, position 73,762,205. Clinical significance in the table: Likely benign.

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Reference-table entries

ALMS1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:73762205
Cytoband: 2p13.1
HGVS: NM_001378454.1(ALMS1):c.9907+129T>G
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.