chr5:131744574:T>C Detail (hg19)

Information

Genome

Assembly Position
hg19 chr5:131,744,574-131,744,574
hg38 chr5:132,408,882-132,408,882 View the variant detail on this assembly version.

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.342
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[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
0.125 Fibrinogen Adverse Event Novel loci, including those related to Crohn disease, psoriasis, and inflammatio... GWASCAT 20031577 Detail
0.122 Fibrinogen Adverse Event [A genome-wide survey of the human genome identifies novel loci related to commo... GAD 20031577 Detail
0.002 Fibrinogen Adverse Event [A genome-wide survey of the human genome identifies novel loci related to commo... GAD 20031577 Detail
0.005 Fibrinogen Adverse Event [Novel loci, including those related to Crohn disease, psoriasis, and inflammati... GAD 20031577 Detail
0.125 Fibrinogen Adverse Event [A genome-wide survey of the human genome identifies novel loci related to commo... GAD 20031577 Detail
Annotation

Annotations

DescrptionSourceLinks
Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a g... DisGeNET Detail
[A genome-wide survey of the human genome identifies novel loci related to common chronic inflammato... DisGeNET Detail
[A genome-wide survey of the human genome identifies novel loci related to common chronic inflammato... DisGeNET Detail
[Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a ... DisGeNET Detail
[A genome-wide survey of the human genome identifies novel loci related to common chronic inflammato... DisGeNET Detail
Gene
-
dbSNP
rs1016988 dbSNP
Genome
hg19
Position
chr5:131,744,574-131,744,574
Variant Type
snv
Reference Allele
T
Alternative Allele
C
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs1016988
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.3415
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
5723
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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