chr10:26216567:A>G Detail (hg38)

Information

Genome

Assembly Position
hg19 chr10:26,505,496-26,505,496 View the variant detail on this assembly version.
hg38 chr10:26,216,567-26,216,567

HGVS

[No Data.]
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.418
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[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
0.152 schizophrenia Using the multifactor-dimensionality reduction method (MDR), we found that the i... BeFree 17412563 Detail
0.134 schizophrenia Using the multifactor-dimensionality reduction method (MDR), we found that the i... BeFree 17412563 Detail
Annotation

Annotations

DescrptionSourceLinks
Using the multifactor-dimensionality reduction method (MDR), we found that the interactions among th... DisGeNET Detail
Using the multifactor-dimensionality reduction method (MDR), we found that the interactions among th... DisGeNET Detail
Gene
-
dbSNP
rs2236418 dbSNP
Genome
hg38
Position
chr10:26,216,567-26,216,567
Variant Type
snv
Reference Allele
A
Alternative Allele
G
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs2236418
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.4178
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
7003
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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