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rs2231095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2231095(C;C)
Make rs2231095(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944331
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2231095
ebirs2231095
HLIrs2231095
Exacrs2231095
Varsomers2231095
Maprs2231095
PheGenIrs2231095
hapmaprs2231095
1000 genomesrs2231095
hgdprs2231095
ensemblrs2231095
gopubmedrs2231095
geneviewrs2231095
scholarrs2231095
googlers2231095
pharmgkbrs2231095
gwascentralrs2231095
openSNPrs2231095
23andMers2231095
23andMe allrs2231095
SNP Nexus

SNPshotrs2231095
SNPdbers2231095
MSV3drs2231095
GWAS Ctlgrs2231095
Max Magnitude0
ClinVar
Risk rs2231095(A,C,T;A,C,T)
Alt rs2231095(A,C,T;A,C,T)
Reference rs2231095(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912108G>A; NC_000006.11:g.29912108G>C; NC_000006.11:g.29912108G>T
CLNSRC
CLNACC


GET Evidence
HLA-A-E277Q
aa_change Glu277Gln
aa_change_short E277Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.469681
summary