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rs41540615

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41540615(C;T)
Make rs41540615(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943335
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41540615
ebirs41540615
HLIrs41540615
Exacrs41540615
Varsomers41540615
Maprs41540615
PheGenIrs41540615
hapmaprs41540615
1000 genomesrs41540615
hgdprs41540615
ensemblrs41540615
gopubmedrs41540615
geneviewrs41540615
scholarrs41540615
googlers41540615
pharmgkbrs41540615
gwascentralrs41540615
openSNPrs41540615
23andMers41540615
23andMe allrs41540615
SNP Nexus

SNPshotrs41540615
SNPdbers41540615
MSV3drs41540615
GWAS Ctlgrs41540615
Max Magnitude0
ClinVar
Risk rs41540615(G,T;G,T)
Alt rs41540615(G,T;G,T)
Reference rs41540615(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911112C>G; NC_000006.11:g.29911112C>T
CLNSRC
CLNACC


GET Evidence
HLA-A-R138E
aa_change Arg138Glu
aa_change_short R138E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0638298
summary