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rs1137160

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1137160(C;C)
Make rs1137160(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944609
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1137160
ebirs1137160
HLIrs1137160
Exacrs1137160
Varsomers1137160
Maprs1137160
PheGenIrs1137160
hapmaprs1137160
1000 genomesrs1137160
hgdprs1137160
ensemblrs1137160
gopubmedrs1137160
geneviewrs1137160
scholarrs1137160
googlers1137160
pharmgkbrs1137160
gwascentralrs1137160
openSNPrs1137160
23andMers1137160
23andMe allrs1137160
SNP Nexus

SNPshotrs1137160
SNPdbers1137160
MSV3drs1137160
GWAS Ctlgrs1137160
GMAF0.1561
Max Magnitude0
ClinVar
Risk rs1137160(C;C)
Alt rs1137160(C;C)
Reference rs1137160(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912386G>C
CLNSRC
CLNACC


GET Evidence
HLA-A-K335N
aa_change Lys335Asn
aa_change_short K335N
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.127796
summary