chr11:27528394:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr11:27,528,394-27,719,718
hg38 chr11:27,506,847-27,698,171 

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 multiple sclerosis NA BeFree Detail
0.120 obesity NA BeFree,GWASCAT Detail
<0.001 Memory impairment NA BeFree Detail
<0.001 Depressive episode, unspecified NA BeFree Detail
<0.001 Depressive episode, unspecified To investigate whether the brain-derived neurotrophic factor (BDNF) polymorphism... BeFree 21037213 Detail
<0.001 Lewy Body Disease NA BeFree Detail
<0.001 acute disseminated encephalitis NA BeFree Detail
<0.001 borderline personality disorder NA BeFree Detail
<0.001 bronchopulmonary dysplasia NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
To investigate whether the brain-derived neurotrophic factor (BDNF) polymorphism (rs6265, Val66Met) ... 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
rs386602118 dbSNP
Genome
hg19
Position
chr11:27,528,394-27,719,718
Variant Type
snv
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