chr7:101126430:A>G Detail (hg38)

Information

Genome

Assembly Position
hg19 chr7:100,769,711-100,769,711 View the variant detail on this assembly version.
hg38 chr7:101,126,430-101,126,430

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
0.005 Hepatitis C, Chronic The aim of this work was to establish an association between the single-nucleoti... BeFree 23941979 Detail
0.002 Fibrosis, Liver The aim of this work was to establish an association between the single-nucleoti... BeFree 23941979 Detail
0.005 Hepatitis C, Chronic The aim of this work was to establish an association between the single-nucleoti... BeFree 23941979 Detail
0.002 Fibrosis, Liver The aim of this work was to establish an association between the single-nucleoti... BeFree 23941979 Detail
0.036 Hepatitis C, Chronic The aim of this work was to establish an association between the single-nucleoti... BeFree 23941979 Detail
0.001 Virus Diseases The aim of this work was to establish an association between the single-nucleoti... BeFree 23941979 Detail
0.107 colorectal cancer Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs179988... BeFree 21422408 Detail
0.002 eclampsia Association between the SERPINE1 (PAI-1) 4G/5G insertion/deletion promoter polym... BeFree 23180602 Detail
0.011 colorectal cancer Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs179988... BeFree 21422408 Detail
0.004 colorectal carcinoma Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs179988... BeFree 21422408 Detail
0.006 Alzheimer's disease The purpose of this study was to explore the association between the SERPINE1 pr... BeFree 22503724 Detail
0.005 colorectal cancer Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs179988... BeFree 21422408 Detail
<0.001 colorectal carcinoma Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs179988... BeFree 21422408 Detail
0.006 cerebral infarction rs1799889 was associated with CSF PAI-1 concentrations (P = 0.048), and white pa... BeFree 24248324 Detail
0.026 colorectal carcinoma Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs179988... BeFree 21422408 Detail
Annotation

Annotations

DescrptionSourceLinks
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... DisGeNET Detail
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... DisGeNET Detail
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... DisGeNET Detail
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... DisGeNET Detail
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... DisGeNET Detail
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... DisGeNET Detail
Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs1799889), MTHFR 677C&gt;T ... DisGeNET Detail
Association between the SERPINE1 (PAI-1) 4G/5G insertion/deletion promoter polymorphism (rs1799889) ... DisGeNET Detail
Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs1799889), MTHFR 677C&gt;T ... DisGeNET Detail
Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs1799889), MTHFR 677C&gt;T ... DisGeNET Detail
The purpose of this study was to explore the association between the SERPINE1 promoter polymorphisms... DisGeNET Detail
Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs1799889), MTHFR 677C&gt;T ... DisGeNET Detail
Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs1799889), MTHFR 677C&gt;T ... DisGeNET Detail
rs1799889 was associated with CSF PAI-1 concentrations (P = 0.048), and white patients homozygous fo... DisGeNET Detail
Factor V Leiden (rs6025), prothrombin G20210A (rs1799963), PAI-1 4G/5G (rs1799889), MTHFR 677C&gt;T ... DisGeNET Detail
Gene
-
dbSNP
rs1799889 dbSNP
Genome
hg38
Position
chr7:101,126,430-101,126,430
Variant Type
snv
Reference Allele
A
Alternative Allele
G
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