chr17:45800588:A>G Detail (hg38) (CRHR1, LINC02210-CRHR1)

Information

Genome

Assembly Position
hg19 chr17:43,877,954-43,877,954 View the variant detail on this assembly version.
hg38 chr17:45,800,588-45,800,588

HGVS

Type Transcript Protein
RefSeq NM_004382.4:c.34-6422A>G
NM_001145147.1:c.34-6422A>G
NM_001145146.1:c.34-6422A>G
Type Transcript Protein
RefSeq NM_001256299.2:c.-492-6422A>G
Ensemble ENST00000634540.1:c.-492-6422A>G
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
Type Database ID Link
Gene MIM 122561 OMIM
HGNC 2357 HGNC
Ensembl ENSG00000120088 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv399195718 TogoVar
COSMIC
MONDO
Type Database ID Link
Gene MIM
HGNC 51483 HGNC
Ensembl ENSG00000263715 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv399195718 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 generalized anxiety disorder Only rs4792888 in CRHR1 showed modest evidence of association with duloxetine re... BeFree 22249355 Detail
0.127 major depressive disorder Only rs4792888 in CRHR1 showed modest evidence of association with duloxetine re... BeFree 22249355 Detail
0.002 Unipolar Depression Only rs4792888 in CRHR1 showed modest evidence of association with duloxetine re... BeFree 22249355 Detail
Annotation

Annotations

DescrptionSourceLinks
Only rs4792888 in CRHR1 showed modest evidence of association with duloxetine response in MDD (P=0.0... DisGeNET Detail
Only rs4792888 in CRHR1 showed modest evidence of association with duloxetine response in MDD (P=0.0... DisGeNET Detail
Only rs4792888 in CRHR1 showed modest evidence of association with duloxetine response in MDD (P=0.0... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs4792888 dbSNP
Genome
hg38
Position
chr17:45,800,588-45,800,588
Variant Type
snv
Reference Allele
A
Alternative Allele
G
Genome browser