chr15:71096952:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr15:71,389,291-72,075,722 
hg38 chr15:71,096,952-71,783,383

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
0.003 Chronic Obstructive Airway Disease Recent genome-wide association studies have shown associations between variants ... BeFree,GAD 24286382 Detail
0.003 osteoporosis NA BeFree,LHGDN Detail
0.002 Osteoporosis, Postmenopausal NA GAD Detail
0.005 Tobacco use disorder NA GAD Detail
0.120 Substance-Related Disorders NA CTD_human Detail
0.002 Menopause present (finding) NA GAD Detail
0.122 Pulmonary function (finding) NA GAD,GWASCAT Detail
0.003 Chronic Obstructive Airway Disease We included three SNPs previously associated with COPD: rs7671167 (FAM13A), rs13... BeFree 22461431 Detail
Annotation

Annotations

DescrptionSourceLinks
Recent genome-wide association studies have shown associations between variants at five loci (TNS1, ... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
We included three SNPs previously associated with COPD: rs7671167 (FAM13A), rs13180 (IREB2), and rs8... 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
rs17096090 dbSNP
Genome
hg38
Position
chr15:71,096,952-71,783,383
Variant Type
snv
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