chr1:67215986:T>G Detail (hg38) (IL23R, C1orf141)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr1:67,681,669-67,681,669 View the variant detail on this assembly version. |
hg38 | chr1:67,215,986-67,215,986 |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001276351.1:c.-104+15860A>C | |
Ensemble | ENST00000371007.6:c.-104+15860A>C |
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_144701.2:c.799-3588T>G | |
Ensemble | ENST00000347310.10:c.799-3588T>G | |
ENST00000425614.3:c.34-3588T>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:0.443 | |
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 |
---|---|---|---|---|---|
0.327 | ulcerative colitis | IL-23 receptor gene rs7517847 and rs1004819 SNPs in ulcerative colitis. | BeFree | 22735800 | Detail |
0.013 | rheumatoid arthritis | Association of interleukin 23 receptor gene polymorphisms (rs10489629, rs7517847... | BeFree | 22718508 | Detail |
0.371 | Crohn Disease | Genome-wide association study identifies new susceptibility loci for Crohn disea... | GWASCAT | 17435756 | Detail |
0.371 | Crohn Disease | The data show an association of both IL23R SNPs with overall IBD (statistically ... | BeFree | 18383521 | Detail |
0.327 | ulcerative colitis | The data show an association of both IL23R SNPs with overall IBD (statistically ... | BeFree | 18383521 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
IL-23 receptor gene rs7517847 and rs1004819 SNPs in ulcerative colitis. | DisGeNET | Detail |
Association of interleukin 23 receptor gene polymorphisms (rs10489629, rs7517847) with rheumatoid ar... | DisGeNET | Detail |
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates au... | DisGeNET | Detail |
The data show an association of both IL23R SNPs with overall IBD (statistically stronger, rs7517847;... | DisGeNET | Detail |
The data show an association of both IL23R SNPs with overall IBD (statistically stronger, rs7517847;... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs7517847 dbSNP
- Genome
- hg38
- Position
- chr1:67,215,986-67,215,986
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- G
- 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))
- rs7517847
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.4426
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 7418
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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