Variant (rsID / SNP)

rs200826787

rs200826787 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALMS1. Location: chromosome 2, position 73,761,999. Clinical significance in the table: Uncertain significance.

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Reference-table entries

ALMS1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:73761999
Cytoband: 2p13.1
HGVS: NM_001378454.1(ALMS1):c.9830A>G (p.Tyr3277Cys)
Allele change: Missense_Y3276C

Associated conditions / phenotypes

Alstrom syndrome

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.