chr9:22010412:A>G Detail (hg19)

Information

Genome

Assembly Position
hg19 chr9:22,010,412-22,010,412
hg38 chr9:22,010,413-22,010,413 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

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
0.322 Diabetes Mellitus, Non-Insulin-Dependent The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six varia... BeFree 20384434 Detail
0.452 Diabetes Mellitus, Non-Insulin-Dependent The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six varia... BeFree 20384434 Detail
0.010 Impaired glucose tolerance The analyses showed that age (P < 0.0001), BMI (P < 0.0001), and six varia... BeFree 20384434 Detail
<0.001 Impaired glucose tolerance The analyses showed that age (P &lt; 0.0001), BMI (P &lt; 0.0001), and six varia... BeFree 20384434 Detail
0.083 Diabetes Mellitus, Non-Insulin-Dependent [Our results suggest that combining genetic markers with traditional clinical ri... GAD 20384434 Detail
0.002 Glucose Metabolism Disorders [Our results suggest that combining genetic markers with traditional clinical ri... GAD 20384434 Detail
Annotation

Annotations

DescrptionSourceLinks
The analyses showed that age (P &lt; 0.0001), BMI (P &lt; 0.0001), and six variants (IGF2BP2 rs44029... DisGeNET Detail
The analyses showed that age (P &lt; 0.0001), BMI (P &lt; 0.0001), and six variants (IGF2BP2 rs44029... DisGeNET Detail
The analyses showed that age (P &lt; 0.0001), BMI (P &lt; 0.0001), and six variants (IGF2BP2 rs44029... DisGeNET Detail
The analyses showed that age (P &lt; 0.0001), BMI (P &lt; 0.0001), and six variants (IGF2BP2 rs44029... DisGeNET Detail
[Our results suggest that combining genetic markers with traditional clinical risk factors has the p... DisGeNET Detail
[Our results suggest that combining genetic markers with traditional clinical risk factors has the p... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs495490 dbSNP
Genome
hg19
Position
chr9:22,010,412-22,010,412
Variant Type
snv
Reference Allele
A
Alternative Allele
G
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