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

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
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

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
Gene
-
dbSNP
rs7538501 dbSNP
Genome
hg38
Position
chr1:196,932,623-196,932,623
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Genome browser