chr11:102715947:>A Detail (hg19)

Information

Genome

Assembly Position
hg19 chr11:102,715,947-102,715,947
hg38 chr11:102,845,216-102,845,216 

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
0.005 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
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
Gene
-
dbSNP
rs35068180 dbSNP
Genome
hg19
Position
chr11:102,715,947-102,715,947
Variant Type
snv
Reference Allele
-
Alternative Allele
A
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