chr11:60088664:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr11:59,856,137-59,865,940 
hg38 chr11:60,088,664-60,098,467

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
0.002 brain ischemia NA GAD Detail
0.002 Chlamydia Infections NA GAD Detail
<0.001 colorectal carcinoma NA BeFree Detail
0.003 Dermatitis, Atopic NA BeFree,GAD Detail
0.005 Diabetes Mellitus, Non-Insulin-Dependent NA GAD Detail
0.122 drug allergy NA CTD_human,GAD Detail
0.003 Eczema NA BeFree,GAD Detail
0.002 Eosinophilia NA GAD Detail
0.002 Hodgkin Disease NA GAD Detail
0.122 Immediate hypersensitivity NA CTD_human,GAD Detail
0.009 Inflammation NA GAD Detail
0.002 periodontitis NA GAD Detail
0.005 pneumonia NA GAD,LHGDN Detail
0.002 Respiratory Syncytial Virus Infections NA GAD Detail
0.055 asthma To investigate whether the single-nucleotide polymorphisms (SNPs) Ile75Val and G... BeFree 22533235 Detail
0.002 Cerebrovascular accident NA GAD Detail
0.002 trachoma NA GAD Detail
0.002 urticaria NA GAD Detail
<0.001 Vitamin D Deficiency NA BeFree Detail
<0.001 Wheezing NA BeFree Detail
0.002 Bronchial Hyperreactivity NA GAD Detail
<0.001 allergic asthma NA BeFree Detail
<0.001 Childhood asthma NA BeFree Detail
0.014 Atopy NA GAD Detail
<0.001 Childhood asthma The 6 loci (IL-13 C-1112T, IL-13 C1923T, IL-4 C-590T, IL-4RA 175V, FcER1B E237G ... BeFree 19862939 Detail
0.055 asthma Association of the MS4A2 gene promoter C-109T or the 7th exon E237G polymorphism... BeFree 24495860 Detail
0.055 asthma CD14-159 C/T and MS4A2 Glu237Gly were identified to have difference in genotype/... BeFree 18931892 Detail
<0.001 allergic asthma Data indicated that the MS4A2 gene E237G variant may be a risk factor for develo... BeFree 24495860 Detail
0.122 Asthma, Aspirin-Induced NA CTD_human,GAD Detail
<0.001 colorectal cancer NA BeFree Detail
0.120 IgE responsiveness, atopic NA CTD_human Detail
0.002 coronary artery disease NA GAD Detail
0.002 Precursor Cell Lymphoblastic Leukemia Lymphoma NA GAD Detail
0.002 granulomatosis with polyangiitis NA GAD Detail
0.001 Allergic disposition NA BeFree Detail
<0.001 Allergic sensitization NA BeFree Detail
0.002 atherosclerosis NA GAD Detail
0.002 Bronchiolitis, Viral NA GAD 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
To investigate whether the single-nucleotide polymorphisms (SNPs) Ile75Val and Gln576Arg in the IL4R... 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
The 6 loci (IL-13 C-1112T, IL-13 C1923T, IL-4 C-590T, IL-4RA 175V, FcER1B E237G and 12-ADR Q27E) mak... DisGeNET Detail
Association of the MS4A2 gene promoter C-109T or the 7th exon E237G polymorphisms with asthma risk: ... DisGeNET Detail
CD14-159 C/T and MS4A2 Glu237Gly were identified to have difference in genotype/allele frequencies b... DisGeNET Detail
Data indicated that the MS4A2 gene E237G variant may be a risk factor for developing atopic asthma a... 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
rs386599440 dbSNP
Genome
hg38
Position
chr11:60,088,664-60,098,467
Variant Type
snv
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