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rs1137631

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1137631(A;A)
Make rs1137631(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945260
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1137631
ebirs1137631
HLIrs1137631
Exacrs1137631
Varsomers1137631
Maprs1137631
PheGenIrs1137631
hapmaprs1137631
1000 genomesrs1137631
hgdprs1137631
ensemblrs1137631
gopubmedrs1137631
geneviewrs1137631
scholarrs1137631
googlers1137631
pharmgkbrs1137631
gwascentralrs1137631
openSNPrs1137631
23andMers1137631
23andMe allrs1137631
SNP Nexus

SNPshotrs1137631
SNPdbers1137631
MSV3drs1137631
GWAS Ctlgrs1137631
GMAF0.1887
Max Magnitude0
ClinVar
Risk rs1137631(A;A)
Alt rs1137631(A;A)
Reference rs1137631(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29913037G>A
CLNSRC
CLNACC


GET Evidence
HLA-A-V358M
aa_change Val358Met
aa_change_short V358M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.168619
summary