chr11:636496:A>G Detail (hg19)

Information

Genome

Assembly Position
hg19 chr11:636,496-636,496
hg38 chr11:636,496-636,496 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

JP HGVD:[No Data.]
ToMMo:0.791
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
0.014 Psychotic Disorders Linkage between the DRD4 and COMT genes and cognitive measures characterizing ve... BeFree 17763983 Detail
0.226 schizophrenia Linkage between the DRD4 and COMT genes and cognitive measures characterizing ve... BeFree 17763983 Detail
Annotation

Annotations

DescrptionSourceLinks
Linkage between the DRD4 and COMT genes and cognitive measures characterizing verbal memory, executi... DisGeNET Detail
Linkage between the DRD4 and COMT genes and cognitive measures characterizing verbal memory, executi... DisGeNET Detail
Gene
-
dbSNP
rs936461 dbSNP
Genome
hg19
Position
chr11:636,496-636,496
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))
rs936461
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.7908
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
13249
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16754
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