chr15:21145734:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr15:21,145,734-21,212,685
hg38 chr15:20,940,405-21,007,356 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 squamous cell carcinoma NA BeFree Detail
0.002 celiac disease NA BeFree Detail
<0.001 Malignant tumor of cervix NA BeFree Detail
<0.001 Primary biliary cirrhosis NA BeFree Detail
<0.001 ulcerative colitis NA BeFree Detail
<0.001 Dermatitis, Atopic NA BeFree Detail
0.002 Diabetes Mellitus, Insulin-Dependent NA BeFree Detail
<0.001 Eczema NA BeFree Detail
<0.001 Disorder of eye NA BeFree Detail
<0.001 membranous glomerulonephritis NA BeFree Detail
<0.001 Inflammatory Bowel Diseases NA BeFree Detail
<0.001 arthropathy NA BeFree Detail
<0.001 Leukemia, Myelocytic, Acute NA BeFree Detail
<0.001 Lupus Erythematosus, Systemic NA BeFree Detail
<0.001 multiple sclerosis NA BeFree Detail
<0.001 lipoid nephrosis NA BeFree Detail
<0.001 systemic scleroderma We also report the significant association of the -1661A/G genotype, -1661 & -31... BeFree 24801647 Detail
<0.001 thromboangiitis obliterans NA BeFree Detail
<0.001 Uveomeningoencephalitic Syndrome NA BeFree Detail
<0.001 vasculitis NA BeFree Detail
<0.001 Bronchial Hyperreactivity NA BeFree Detail
<0.001 acute leukemia NA BeFree Detail
<0.001 Primary Sj�gren's syndrome NA BeFree Detail
<0.001 allergic asthma NA BeFree Detail
<0.001 acute intermittent porphyria NA BeFree Detail
<0.001 Niemann-Pick disease, type C NA BeFree Detail
<0.001 Childhood asthma NA BeFree Detail
<0.001 Postpartum Thyroiditis NA BeFree Detail
<0.001 cervical squamous cell carcinoma NA BeFree Detail
<0.001 cervix carcinoma NA BeFree Detail
<0.001 Thyroid associated opthalmopathies NA BeFree Detail
<0.001 pricking of skin NA BeFree Detail
0.002 Diabetes Mellitus, Insulin-Dependent We assessed the association of five SNPs present in the CTLA-4 gene [-318C/T, -1... BeFree 16671945 Detail
<0.001 breast carcinoma NA BeFree Detail
<0.001 skin carcinoma NA BeFree Detail
0.001 Acute GVH disease NA BeFree Detail
<0.001 Glomerulonephritis, Minimal Change NA BeFree Detail
<0.001 Juvenile arthritis NA BeFree Detail
<0.001 juvenile rheumatoid arthritis NA BeFree Detail
<0.001 Experimental Organism Basal Cell Carcinoma NA BeFree Detail
0.001 rheumatoid arthritis NA BeFree Detail
<0.001 asthma NA BeFree Detail
0.001 Autoimmune Diseases NA BeFree Detail
<0.001 Malignant neoplasm of breast NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
We also report the significant association of the -1661A/G genotype, -1661 & -319 AC-GT diplotype an... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
We assessed the association of five SNPs present in the CTLA-4 gene [-318C/T, -1661A/G and -1722C/T ... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs386609373 dbSNP
Genome
hg19
Position
chr15:21,145,734-21,212,685
Variant Type
snv
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