chr20:44748099:C>A Detail (hg19) (CD40)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr20:44,748,099-44,748,099 |
hg38 | chr20:46,119,460-46,119,460 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_152854.3:c.51+1066C>A | |
NM_001250.5:c.51+1066C>A | ||
NM_001302753.1:c.51+1066C>A |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.004 | arteriosclerosis | Also, the CD40 rs1535045 gene variant may influence development of subclinical a... | BeFree | 23166616 | Detail |
0.006 | rheumatoid arthritis | One thousand five hundred and seventy-five patients fulfilling the 1987 ACR clas... | BeFree | 23166616 | Detail |
0.006 | arteriosclerosis | Although we did not observe a significant association of CD40-CD154 gene variant... | BeFree | 23166616 | Detail |
0.104 | atherosclerosis | Although we did not observe a significant association of CD40-CD154 gene variant... | BeFree | 23166616 | Detail |
0.092 | atherosclerosis | Also, the CD40 rs1535045 gene variant may influence development of subclinical a... | BeFree | 23166616 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Also, the CD40 rs1535045 gene variant may influence development of subclinical atherosclerosis in RA... | DisGeNET | Detail |
One thousand five hundred and seventy-five patients fulfilling the 1987 ACR classification criteria ... | DisGeNET | Detail |
Although we did not observe a significant association of CD40-CD154 gene variants with the developme... | DisGeNET | Detail |
Although we did not observe a significant association of CD40-CD154 gene variants with the developme... | DisGeNET | Detail |
Also, the CD40 rs1535045 gene variant may influence development of subclinical atherosclerosis in RA... | DisGeNET | Detail |
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- dbSNP
- rs1535045 dbSNP
- Genome
- hg19
- Position
- chr20:44,748,099-44,748,099
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- A
Genome browser