rs8904

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs8904(C;T)

Make rs8904(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

35402011

Gene

NFKBIA

is a	snp
is	mentioned by
dbSNP	rs8904
dbSNP (classic)	rs8904
ClinGen	rs8904
ebi	rs8904
HLI	rs8904
Exac	rs8904
Gnomad	rs8904
Varsome	rs8904
LitVar	rs8904
Map	rs8904
PheGenI	rs8904
Biobank	rs8904
1000 genomes	rs8904
hgdp	rs8904
ensembl	rs8904
geneview	rs8904
scholar	rs8904
google	rs8904
pharmgkb	rs8904
gwascentral	rs8904
openSNP	rs8904
23andMe	rs8904
SNPshot	rs8904
SNPdbe	rs8904
MSV3d	rs8904
GWAS Ctlg	rs8904

GMAF

0.4233

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 19773451 ] Role of inflammation gene polymorphisms on pain severity in lung cancer patients

[PMID 16380906 ] Genomewide high-density SNP linkage analysis of 236 Japanese families supports the existence of schizophrenia susceptibility loci on chromosomes 1p, 14q, and 20p.

[PMID 18635889 ] Toll-like receptor 1 polymorphisms affect innate immune responses and outcomes in sepsis.

[PMID 19223558 ] Polymorphic variation in NFKB1 and other aspirin-related genes and risk of Hodgkin lymphoma.

[PMID 19500386 ] Polymorphisms in NF-kappaB inhibitors and risk of epithelial ovarian cancer.

[PMID 20811626 ] Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.

[PMID 23176038] Evaluation of NFKB1A variants in patients with knee osteoarthritis.

ClinVar
Risk	rs8904(T;T)
Alt	rs8904(T;T)
Reference	Rs8904(C;C)
Significance	Non-pathogenic
Disease	Ectodermal dysplasia not specified
Variation	info
Gene	NFKBIA
CLNDBN	Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant not specified
Reversed	1
HGVS	NC_000014.8:g.35871217G>A
CLNSRC
CLNACC	RCV000274336.1, RCV000455898.1,