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rs2230954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2230954(C;T)
Make rs2230954(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942594
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2230954
ebirs2230954
HLIrs2230954
Exacrs2230954
Varsomers2230954
Maprs2230954
PheGenIrs2230954
hapmaprs2230954
1000 genomesrs2230954
hgdprs2230954
ensemblrs2230954
gopubmedrs2230954
geneviewrs2230954
scholarrs2230954
googlers2230954
pharmgkbrs2230954
gwascentralrs2230954
openSNPrs2230954
23andMers2230954
23andMe allrs2230954
SNP Nexus

SNPshotrs2230954
SNPdbers2230954
MSV3drs2230954
GWAS Ctlgrs2230954
GMAF0.1359
Max Magnitude0
ClinVar
Risk rs2230954(T;T)
Alt rs2230954(T;T)
Reference rs2230954(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910371C>T
CLNSRC
CLNACC


[PMID 19774073OA-icon.png] Genetic epidemiology of glioblastoma multiforme: confirmatory and new findings from analyses of human leukocyte antigen alleles and motifs.

GET Evidence
HLA-A-S14L
aa_change Ser14Leu
aa_change_short S14L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.131187
summary