chr11:59855711:T>C Detail (hg19)

Information

Genome

Assembly Position
hg19 chr11:59,855,711-59,855,711
hg38 chr11:60,088,238-60,088,238 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:0.148
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
0.055 asthma To investigate associations between total serum immunoglobulin E (IgE) levels an... BeFree 22376040 Detail
0.038 asthma To investigate associations between total serum immunoglobulin E (IgE) levels an... BeFree 22376040 Detail
0.266 asthma To investigate associations between total serum immunoglobulin E (IgE) levels an... BeFree 22376040 Detail
Annotation

Annotations

DescrptionSourceLinks
To investigate associations between total serum immunoglobulin E (IgE) levels and single nucleotide ... DisGeNET Detail
To investigate associations between total serum immunoglobulin E (IgE) levels and single nucleotide ... DisGeNET Detail
To investigate associations between total serum immunoglobulin E (IgE) levels and single nucleotide ... DisGeNET Detail
Gene
-
dbSNP
rs1441585 dbSNP
Genome
hg19
Position
chr11:59,855,711-59,855,711
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))
rs1441585
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.1481
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
2482
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16758
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