chr8:145133551:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr8:145,133,551-145,135,551
hg38 chr8:144,078,648-144,080,648 

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 renal cell carcinoma NA BeFree Detail
<0.001 Cardiovascular Diseases NA BeFree Detail
<0.001 colorectal carcinoma NA BeFree Detail
<0.001 Coronary Arteriosclerosis NA BeFree Detail
0.001 Coronary heart disease NA BeFree Detail
0.003 Diabetes NA BeFree Detail
0.003 diabetes mellitus NA BeFree Detail
<0.001 Diabetic Nephropathy NA BeFree Detail
<0.001 eclampsia NA BeFree Detail
0.002 obesity Furthermore, four genes (FZD7, PRLHR, EXOSC4, and EIF6) with differential promot... BeFree 25871514 Detail
0.003 Diabetes Mellitus, Non-Insulin-Dependent By using a Cox proportional hazard model, common variants in the PPARG (P12A), C... BeFree 17570749 Detail
0.003 Diabetes Mellitus, Non-Insulin-Dependent The P12A variant in the PPARG gene and the E23K polymorphism in KCNJ11 are both ... BeFree 17994213 Detail
0.003 Diabetes Mellitus, Non-Insulin-Dependent In contrast, the well-documented associations of peroxisome proliferator-activat... BeFree 15561965 Detail
<0.001 pancreatic carcinoma NA BeFree Detail
<0.001 Dyslipidemias NA BeFree Detail
<0.001 Impaired glucose tolerance NA BeFree Detail
<0.001 Malignant neoplasm of pancreas NA BeFree Detail
<0.001 endometrial carcinoma NA BeFree Detail
0.001 Metabolic syndrome X NA BeFree Detail
<0.001 Carotid Atherosclerosis NA BeFree Detail
<0.001 colorectal cancer NA BeFree Detail
<0.001 Insulin resistance syndrome 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
Furthermore, four genes (FZD7, PRLHR, EXOSC4, and EIF6) with differential promoter methylation were ... DisGeNET Detail
By using a Cox proportional hazard model, common variants in the PPARG (P12A), CAPN10 (SNP43 and 44)... DisGeNET Detail
The P12A variant in the PPARG gene and the E23K polymorphism in KCNJ11 are both known to influence i... DisGeNET Detail
In contrast, the well-documented associations of peroxisome proliferator-activated receptor gamma P1... 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
rs386597997 dbSNP
Genome
hg19
Position
chr8:145,133,551-145,135,551
Variant Type
snv
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