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rs66772001

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs66772001(A;A)
Make rs66772001(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269556
GeneHLA-C
is asnp
is mentioned by
dbSNPrs66772001
ebirs66772001
HLIrs66772001
Exacrs66772001
Varsomers66772001
Maprs66772001
PheGenIrs66772001
hapmaprs66772001
1000 genomesrs66772001
hgdprs66772001
ensemblrs66772001
gopubmedrs66772001
geneviewrs66772001
scholarrs66772001
googlers66772001
pharmgkbrs66772001
gwascentralrs66772001
openSNPrs66772001
23andMers66772001
23andMe allrs66772001
SNP Nexus

SNPshotrs66772001
SNPdbers66772001
MSV3drs66772001
GWAS Ctlgrs66772001
GMAF0.2208
Max Magnitude0
ClinVar
Risk rs66772001(A;A)
Alt rs66772001(A;A)
Reference rs66772001(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237333T>A
CLNSRC
CLNACC