chr6:31575318:G>A Detail (hg38)

Information

Genome

Assembly Position
hg19 chr6:31,543,095-31,543,095 View the variant detail on this assembly version.
hg38 chr6:31,575,318-31,575,318

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
0.003 Migraine Disorders Regarding any history of migraine, the multivariable-adjusted odds ratios (95% c... BeFree 19559392 Detail
0.123 Migraine Disorders Regarding any history of migraine, the multivariable-adjusted odds ratios (95% c... BeFree 19559392 Detail
0.139 Migraine Disorders Regarding any history of migraine, the multivariable-adjusted odds ratios (95% c... BeFree 19559392 Detail
0.139 Migraine Disorders [Variants in TNF, CCR2, TGFB1, NOS3, and IL9 were found to be associated with mi... GAD 19559392 Detail
Annotation

Annotations

DescrptionSourceLinks
Regarding any history of migraine, the multivariable-adjusted odds ratios (95% confidence intervals)... DisGeNET Detail
Regarding any history of migraine, the multivariable-adjusted odds ratios (95% confidence intervals)... DisGeNET Detail
Regarding any history of migraine, the multivariable-adjusted odds ratios (95% confidence intervals)... DisGeNET Detail
[Variants in TNF, CCR2, TGFB1, NOS3, and IL9 were found to be associated with migraine but did not r... DisGeNET Detail
Gene
-
dbSNP
rs673 dbSNP
Genome
hg38
Position
chr6:31,575,318-31,575,318
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser