chr11:113346251:>G Detail (hg19)

Information

Genome

Assembly Position
hg19 chr11:113,346,251-113,346,251
hg38 chr11:113,475,529-113,475,529 

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

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
0.178 attention deficit hyperactivity disorder We have assessed variants in four genes, DDC (rs3837091 and rs3735273), DRD2 (rs... BeFree 24163823 Detail
0.291 schizophrenia Association between DRD2 (rs1799732 and rs1801028) and ANKK1 (rs1800497) polymor... BeFree 25504812 Detail
0.017 Malignant neoplasm of lung [When numeric scores were assigned to both the SNP and demographic data, and seq... GAD 19789190 Detail
0.009 schizophrenia Association between DRD2 (rs1799732 and rs1801028) and ANKK1 (rs1800497) polymor... BeFree 25504812 Detail
Annotation

Annotations

DescrptionSourceLinks
We have assessed variants in four genes, DDC (rs3837091 and rs3735273), DRD2 (rs1800496, rs1801028, ... DisGeNET Detail
Association between DRD2 (rs1799732 and rs1801028) and ANKK1 (rs1800497) polymorphisms and schizophr... DisGeNET Detail
[When numeric scores were assigned to both the SNP and demographic data, and sequentially combined b... DisGeNET Detail
Association between DRD2 (rs1799732 and rs1801028) and ANKK1 (rs1800497) polymorphisms and schizophr... DisGeNET Detail
Gene
-
dbSNP
rs1799732 dbSNP
Genome
hg19
Position
chr11:113,346,251-113,346,251
Variant Type
snv
Reference Allele
-
Alternative Allele
G
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