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rs3129055

From SNPedia

Orientationminus
Stabilizedminus
Make rs3129055(C;C)
Make rs3129055(C;T)
Make rs3129055(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29702484
is asnp
is mentioned by
dbSNPrs3129055
ebirs3129055
HLIrs3129055
Exacrs3129055
Varsomers3129055
Maprs3129055
PheGenIrs3129055
hapmaprs3129055
1000 genomesrs3129055
hgdprs3129055
ensemblrs3129055
gopubmedrs3129055
geneviewrs3129055
scholarrs3129055
googlers3129055
pharmgkbrs3129055
gwascentralrs3129055
openSNPrs3129055
23andMers3129055
23andMe allrs3129055
SNP Nexus

SNPshotrs3129055
SNPdbers3129055
MSV3drs3129055
GWAS Ctlgrs3129055
GMAF0.2759
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19664746OA-icon.png]
Trait Nasopharyngeal Carcinoma
Title Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21.
Risk Allele G
P-val 7E-11
Odds Ratio 1.51 [1.34-1.71]
OMIM161550
Desc
Variant
Relatedalso


GET Evidence
rs3129055
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.289062
summary