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rs1957106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1957106(A;A)
Make rs1957106(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position35404564
GeneNFKBIA
is asnp
is mentioned by
dbSNPrs1957106
dbSNP (classic)rs1957106
ClinGenrs1957106
ebirs1957106
HLIrs1957106
Exacrs1957106
Gnomadrs1957106
Varsomers1957106
LitVarrs1957106
Maprs1957106
PheGenIrs1957106
Biobankrs1957106
1000 genomesrs1957106
hgdprs1957106
ensemblrs1957106
geneviewrs1957106
scholarrs1957106
googlers1957106
pharmgkbrs1957106
gwascentralrs1957106
openSNPrs1957106
23andMers1957106
SNPshotrs1957106
SNPdbers1957106
MSV3drs1957106
GWAS Ctlgrs1957106
GMAF0.2406
Max Magnitude0

[PMID 19500386OA-icon.png] Polymorphisms in NF-kappaB Inhibitors and Risk of Epithelial Ovarian Cancer


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


[PMID 25215581OA-icon.png] Identification of a NFKBIA polymorphism associated with lower NFKBIA protein levels and poor survival outcomes in patients with glioblastoma multiforme


ClinVar
Risk rs1957106(A;A)
Alt rs1957106(A;A)
Reference Rs1957106(G;G)
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 0
HGVS NC_000014.8:g.35873770G>A
CLNSRC
CLNACC RCV000284527.1, RCV000455089.1,