chr1:154453788:C>T Detail (hg38) (IL6R)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr1:154,426,264-154,426,264 View the variant detail on this assembly version. |
hg38 | chr1:154,453,788-154,453,788 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_181359.2:c.1066+3808C>T | |
NM_000565.3:c.1067-700C>T | ||
Ensemble | ENST00000344086.8:c.1066+3808C>T |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.380 | |
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 |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
<0.001 | Fatigue | The associations between fatigue and SNPs in inflammation-related genes; IL1β (r... | BeFree | 21496483 | Detail |
0.131 | asthma | Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. | GWASCAT | 21907864 | Detail |
<0.001 | asthma | Two loci were confirmed to associate with asthma risk in the replication cohorts... | BeFree | 21907864 | Detail |
0.131 | asthma | [Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.] | GAD | 21907864 | Detail |
0.122 | Fibrinogen Adverse Event | Multiethnic meta-analysis of genome-wide association studies in >100 000 subj... | GWASCAT | 23969696 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
The associations between fatigue and SNPs in inflammation-related genes; IL1β (rs16944), IL6 (rs1800... | DisGeNET | Detail |
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. | DisGeNET | Detail |
Two loci were confirmed to associate with asthma risk in the replication cohorts and reached genome-... | DisGeNET | Detail |
[Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.] | DisGeNET | Detail |
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 f... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs4129267 dbSNP
- Genome
- hg38
- Position
- chr1:154,453,788-154,453,788
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- 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))
- rs4129267
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.3805
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 6377
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
Genome browser