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rs1136695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1136695(A;G)
Make rs1136695(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943287
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136695
ebirs1136695
HLIrs1136695
Exacrs1136695
Varsomers1136695
Maprs1136695
PheGenIrs1136695
hapmaprs1136695
1000 genomesrs1136695
hgdprs1136695
ensemblrs1136695
gopubmedrs1136695
geneviewrs1136695
scholarrs1136695
googlers1136695
pharmgkbrs1136695
gwascentralrs1136695
openSNPrs1136695
23andMers1136695
23andMe allrs1136695
SNP Nexus

SNPshotrs1136695
SNPdbers1136695
MSV3drs1136695
GWAS Ctlgrs1136695
GMAF0.365
Max Magnitude0
ClinVar
Risk rs1136695(G;G)
Alt rs1136695(G;G)
Reference rs1136695(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911064A>G
CLNSRC
CLNACC


GET Evidence
HLA-A-I121M
aa_change Ile121Met
aa_change_short I121M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.484101
summary