Variant (rsID / SNP)

rs45608038

rs45608038 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALMS1. Location: chromosome 2, position 73,679,013. Clinical significance in the table: Benign.

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Reference-table entries

ALMS1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:73679013
Cytoband: 2p13.1
HGVS: NM_001378454.1(ALMS1):c.5359A>G (p.Asn1787Asp)
Allele change: Missense_N1786D

Associated conditions / phenotypes

Alstrom syndrome|Monogenic diabetes

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.