Gene entry
GPSM2
G protein signaling modulator 2
- Chromosome
- 1
- Cytoband
- 1p13.3
- Variants (rsID)
- 20
GPSM2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p13.3). Its official name is “G protein signaling modulator 2”. The reference table lists 20 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs338489Benignsingle nucleotide variantChudley-McCullough syndrome
- rs35089879Benignsingle nucleotide variantChudley-McCullough syndrome
- rs41279678Benignsingle nucleotide variantChudley-McCullough syndrome
- rs705268Benignsingle nucleotide variantChudley-McCullough syndrome
- rs141562079Conflicting interpretationssingle nucleotide variantChudley-McCullough syndrome
- rs201878481Conflicting interpretationssingle nucleotide variantChudley-McCullough syndrome
- rs61754640Conflicting interpretationssingle nucleotide variantChudley-McCullough syndrome
- rs79730689Conflicting interpretationssingle nucleotide variantChudley-McCullough syndrome
- rs528069912PathogenicDeletionChudley-McCullough syndrome|Rare genetic deafness|GPSM2-Related Disorders
- rs772372530PathogenicDeletionGPSM2-Related Disorders|Rare genetic deafness|Chudley-McCullough syndrome
- rs148266178Uncertain significancesingle nucleotide variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.