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rs1136949

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1136949(A;G)
Make rs1136949(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944520
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136949
ebirs1136949
HLIrs1136949
Exacrs1136949
Varsomers1136949
Maprs1136949
PheGenIrs1136949
hapmaprs1136949
1000 genomesrs1136949
hgdprs1136949
ensemblrs1136949
gopubmedrs1136949
geneviewrs1136949
scholarrs1136949
googlers1136949
pharmgkbrs1136949
gwascentralrs1136949
openSNPrs1136949
23andMers1136949
23andMe allrs1136949
SNP Nexus

SNPshotrs1136949
SNPdbers1136949
MSV3drs1136949
GWAS Ctlgrs1136949
GMAF0.1478
Max Magnitude0
ClinVar
Risk rs1136949(G;G)
Alt rs1136949(G;G)
Reference rs1136949(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912297A>G
CLNSRC
CLNACC


GET Evidence
HLA-A-I306V
aa_change Ile306Val
aa_change_short I306V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.118617
summary