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rs45505094

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45505094(A;A)
Make rs45505094(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943311
GeneHLA-A
is asnp
is mentioned by
dbSNPrs45505094
dbSNP (classic)rs45505094
ClinGenrs45505094
ebirs45505094
HLIrs45505094
Exacrs45505094
Gnomadrs45505094
Varsomers45505094
LitVarrs45505094
Maprs45505094
PheGenIrs45505094
Biobankrs45505094
1000 genomesrs45505094
hgdprs45505094
ensemblrs45505094
geneviewrs45505094
scholarrs45505094
googlers45505094
pharmgkbrs45505094
gwascentralrs45505094
openSNPrs45505094
23andMers45505094
SNPshotrs45505094
SNPdbers45505094
MSV3drs45505094
GWAS Ctlgrs45505094
Max Magnitude0
ClinVar
Risk rs45505094(A;A) rs45505094(C;C) rs45505094(T;T)
Alt rs45505094(A;A) rs45505094(C;C) rs45505094(T;T)
Reference Rs45505094(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911088G>A; NC_000006.11:g.29911088G>C; NC_000006.11:g.29911088G>T
CLNSRC
CLNACC