chr17:61565890:>G Detail (hg19) (ACE)

Information

Genome

Assembly Position
hg19 chr17:61,565,890-61,565,890
hg38 chr17:63,488,529-63,488,529 

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
0.203 Kidney Diseases We investigated the association of three ACE gene variants with DN, rs1799752 in... BeFree 19787680 Detail
0.201 Aortic Aneurysm, Thoracic Interestingly, the rs4986790 TLR4 polymorphism confers a higher susceptibility f... BeFree 25120286 Detail
0.201 Aortic Aneurysm, Thoracic Interestingly, the rs4986790 TLR4 polymorphism confers a higher susceptibility f... BeFree 25120286 Detail
0.277 Heart failure We evaluated nuclear factor kappa B {NFkB, rs28362491 [-94ins/delATTG (W/D)]} an... BeFree 23543433 Detail
0.024 congestive heart failure We evaluated nuclear factor kappa B {NFkB, rs28362491 [-94ins/delATTG (W/D)]} an... BeFree 23543433 Detail
<0.001 Aortic Aneurysm, Thoracic Interestingly, the rs4986790 TLR4 polymorphism confers a higher susceptibility f... BeFree 25120286 Detail
Annotation

Annotations

DescrptionSourceLinks
We investigated the association of three ACE gene variants with DN, rs1799752 insertion/deletion (I/... DisGeNET Detail
Interestingly, the rs4986790 TLR4 polymorphism confers a higher susceptibility for sporadic TAA (OR ... DisGeNET Detail
Interestingly, the rs4986790 TLR4 polymorphism confers a higher susceptibility for sporadic TAA (OR ... DisGeNET Detail
We evaluated nuclear factor kappa B {NFkB, rs28362491 [-94ins/delATTG (W/D)]} and angiotensin conver... DisGeNET Detail
We evaluated nuclear factor kappa B {NFkB, rs28362491 [-94ins/delATTG (W/D)]} and angiotensin conver... DisGeNET Detail
Interestingly, the rs4986790 TLR4 polymorphism confers a higher susceptibility for sporadic TAA (OR ... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs1799752 dbSNP
Genome
hg19
Position
chr17:61,565,890-61,565,890
Variant Type
snv
Reference Allele
-
Alternative Allele
G
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