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rs2071592

From SNPedia

Orientationminus
Stabilizedminus
Make rs2071592(A;A)
Make rs2071592(A;T)
Make rs2071592(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31547563
GeneATP6V1G2, ATP6V1G2-DDX39B, LOC100287329, NFKBIL1
is asnp
is mentioned by
dbSNPrs2071592
dbSNP (classic)rs2071592
ClinGenrs2071592
ebirs2071592
HLIrs2071592
Exacrs2071592
Gnomadrs2071592
Varsomers2071592
LitVarrs2071592
Maprs2071592
PheGenIrs2071592
Biobankrs2071592
1000 genomesrs2071592
hgdprs2071592
ensemblrs2071592
geneviewrs2071592
scholarrs2071592
googlers2071592
pharmgkbrs2071592
gwascentralrs2071592
openSNPrs2071592
23andMers2071592
SNPshotrs2071592
SNPdbers2071592
MSV3drs2071592
GWAS Ctlgrs2071592
GMAF0.3893
Max Magnitude0
? (A;A) (A;T) (T;T) 28


[PMID 22210660OA-icon.png] Genetic association study of NF-?B genes in UK Caucasian adult and juvenile onset idiopathic inflammatory myopathy


[PMID 12509789OA-icon.png] Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritis.


[PMID 17517687] Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in Europeans.


[PMID 19578685] Association study between the -62A/T NFKBIL1 polymorphism and obsessive-compulsive disorder.


[PMID 19886988OA-icon.png] Association of polymorphism in genes encoding kappaB inhibitors (IkappaB) with susceptibility to and phenotype of Graves' disease: a case-control study.


[PMID 25809685] Common Variants and Haplotypes in the TF, TNF-α, and TMPRSS6 Genes Are Associated with Iron Status in a Female Black South African Population


[PMID 24896147OA-icon.png] Role of TNF block genetic variants in HIV-associated sensory neuropathy in black Southern Africans