chr2:108602979:> Detail (hg19)

Information

Genome

Assembly Position
hg19 chr2:108,602,979-108,630,450
hg38 chr2:107,986,523-108,013,994 

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 Degenerative polyarthritis Thus, we analyze the expression of members of the organic cation transporter (OC... BeFree 25418136 Detail
0.002 Tobacco use disorder NA GAD Detail
<0.001 Depressive Symptoms NA BeFree Detail
<0.001 Angelman syndrome NA BeFree Detail
<0.001 Recurrent depression NA BeFree Detail
<0.001 Mood Disorders NA BeFree Detail
<0.001 Recurrent depression MPT analyses show significant associations of the norepinephrine transporter (NE... BeFree 18081710 Detail
0.120 Neuropathy, Distal Hereditary Motor, Type VIIA NA CLINVAR Detail
<0.001 rheumatoid arthritis Thus, we analyze the expression of members of the organic cation transporter (OC... BeFree 25418136 Detail
0.080 asthma NA RGD Detail
Annotation

Annotations

DescrptionSourceLinks
Thus, we analyze the expression of members of the organic cation transporter (OCT), of the newly dis... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
MPT analyses show significant associations of the norepinephrine transporter (NET, SLC6A2) -182 T/C ... DisGeNET Detail
NA DisGeNET Detail
Thus, we analyze the expression of members of the organic cation transporter (OCT), of the newly dis... 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
rs386510249 dbSNP
Genome
hg19
Position
chr2:108,602,979-108,630,450
Variant Type
snv
Genome browser