chr10:18129993:G>A Detail (hg19)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr10:18,129,993-18,129,993 |
hg38 | chr10:17,841,064-17,841,064 View the variant detail on this assembly version. |
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 | Leprosy, Multibacillary | However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... | BeFree | 22392581 | Detail |
<0.001 | Leprosy, Multibacillary | However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... | BeFree | 22392581 | Detail |
<0.001 | Leprosy, Paucibacillary | However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... | BeFree | 22392581 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... | DisGeNET | Detail |
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... | DisGeNET | Detail |
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... | DisGeNET | Detail |
- Gene
- -
- dbSNP
- rs692527 dbSNP
- Genome
- hg19
- Position
- chr10:18,129,993-18,129,993
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
Genome browser