chr5:71716480:T>C Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr5:71,012,307-71,012,307 View the variant detail on this assembly version. |
| hg38 | chr5:71,716,480-71,716,480 |
HGVS
[No Data.]
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | 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 |
|---|---|---|---|---|---|
| <0.001 | Chronic schizophrenia | Five CART single nucleotide polymorphisms (SNPs) (rs10515115, rs3763153, rs38573... | BeFree | 24564533 | Detail |
| <0.001 | Chronic schizophrenia | Five CART single nucleotide polymorphisms (SNPs) (rs10515115, rs3763153, rs38573... | BeFree | 24564533 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| Five CART single nucleotide polymorphisms (SNPs) (rs10515115, rs3763153, rs3857384, rs11575893, rs16... | DisGeNET | Detail |
| Five CART single nucleotide polymorphisms (SNPs) (rs10515115, rs3763153, rs3857384, rs11575893, rs16... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs10515115 dbSNP
- Genome
- hg38
- Position
- chr5:71,716,480-71,716,480
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
Genome browser