chr1:196932623:C>T Detail (hg38)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr1:196,901,753-196,901,753 View the variant detail on this assembly version. |
hg38 | chr1:196,932,623-196,932,623 |
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 |
---|---|---|---|---|---|
0.007 | age related macular degeneration | NA | GAD | Detail |
Annotation
Genome browser