chr16:10971020:G>A Detail (hg19) (CIITA)

Information

Genome

Assembly Position
hg19 chr16:10,971,020-10,971,020
hg38 chr16:10,877,163-10,877,163 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

[No Data.]

Prediction

ClinVar

Clinical Significance not provided
Review star
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
not provided no assertion provided not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.016 multiple sclerosis The objective of this study was to investigate the association between the HLA a... BeFree 25992516 Detail
0.001 myocardial infarction A promoter polymorphism (-168A/G, rs3087456) in the MHC2TA gene was associated w... BeFree 17012290 Detail
0.253 rheumatoid arthritis The MHC2TA -168A/G polymorphism and risk for rheumatoid arthritis: a meta-analys... BeFree 17875550 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000246.3(CIITA):c.-168G>A AND not provided ClinVar Detail
The objective of this study was to investigate the association between the HLA alleles at the DQA1, ... DisGeNET Detail
A promoter polymorphism (-168A/G, rs3087456) in the MHC2TA gene was associated with increased suscep... DisGeNET Detail
The MHC2TA -168A/G polymorphism and risk for rheumatoid arthritis: a meta-analysis of 6861 patients ... DisGeNET Detail
Gene
-
dbSNP
rs199476059 dbSNP
Genome
hg19
Position
chr16:10,971,020-10,971,020
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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