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rs1137078

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1137078(A;G)
Make rs1137078(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944571
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1137078
ebirs1137078
HLIrs1137078
Exacrs1137078
Varsomers1137078
Maprs1137078
PheGenIrs1137078
hapmaprs1137078
1000 genomesrs1137078
hgdprs1137078
ensemblrs1137078
gopubmedrs1137078
geneviewrs1137078
scholarrs1137078
googlers1137078
pharmgkbrs1137078
gwascentralrs1137078
openSNPrs1137078
23andMers1137078
23andMe allrs1137078
SNP Nexus

SNPshotrs1137078
SNPdbers1137078
MSV3drs1137078
GWAS Ctlgrs1137078
GMAF0.241
Max Magnitude0
ClinVar
Risk rs1137078(G;G)
Alt rs1137078(G;G)
Reference rs1137078(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912348A>G
CLNSRC
CLNACC


GET Evidence
HLA-A-T323A
aa_change Thr323Ala
aa_change_short T323A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.199495
summary