Variant (rsID / SNP)

rs1042044

rs1042044 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GLP1R. Location: chromosome 6, position 39,041,502. The table records no clinical significance for this variant.

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Reference-table entries

GLP1RNot classified

Variant type: missense_variant
Chromosome / position: 6:39041502
HGVS: NM_002062.5,c.780A>C,p.Leu260Phe
Allele change: Silent

Associated conditions / phenotypes

Mental Depression|Major Depressive Disorder|Depression|Prediabetes Syndrome|Bone Resorption Disease

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.