Gene entry
SIL1
SIL1 nucleotide exchange factor
- Chromosome
- 5
- Cytoband
- 5q31.2
- Variants (rsID)
- 38
SIL1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q31.2). Its official name is “SIL1 nucleotide exchange factor”. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs58624842Benignsingle nucleotide variantMarinesco-Sjögren syndrome
- rs61745568Benignsingle nucleotide variantMarinesco-Sjögren syndrome
- rs115800498Conflicting interpretationssingle nucleotide variantMarinesco-Sjögren syndrome
- rs148927511Conflicting interpretationssingle nucleotide variantMarinesco-Sjögren syndrome
- rs199890503Conflicting interpretationssingle nucleotide variantMarinesco-Sjögren syndrome
- rs61744666Conflicting interpretationssingle nucleotide variantMarinesco-Sjögren syndrome
- rs119456966Pathogenicsingle nucleotide variantMarinesco-Sjögren syndrome
Other listed variants
- rs4835715
- rs6866496
- rs7701116
- rs10039449
- rs11747454
- rs11951084
- rs11958425
- rs13354264
- rs62381232
- rs62381233
- rs62382986
- rs75060853
- rs75401863
- rs75435312
- rs75850692
- rs77147920
- rs77169826
- rs77708058
- rs79143720
- rs80007439
- rs112459130
- rs114009882
- rs114131059
- rs116002613
- rs138622409
- rs141950375
- rs148309019
- rs181409103
- rs185484314
- rs201546394
- rs201636421
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.