chr9:87918231:G>T Detail (hg19)

Information

Genome

Assembly Position
hg19 chr9:87,918,231-87,918,231
hg38 chr9:85,303,316-85,303,316 View the variant detail on this assembly version.

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
0.128 bipolar disorder NA GAD Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
Gene
-
dbSNP
rs2769595 dbSNP
Genome
hg19
Position
chr9:87,918,231-87,918,231
Variant Type
snv
Reference Allele
G
Alternative Allele
T
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