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rs41564222

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41564222(C;G)
Make rs41564222(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356900
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41564222
ebirs41564222
HLIrs41564222
Exacrs41564222
Varsomers41564222
Maprs41564222
PheGenIrs41564222
hapmaprs41564222
1000 genomesrs41564222
hgdprs41564222
ensemblrs41564222
gopubmedrs41564222
geneviewrs41564222
scholarrs41564222
googlers41564222
pharmgkbrs41564222
gwascentralrs41564222
openSNPrs41564222
23andMers41564222
23andMe allrs41564222
SNP Nexus

SNPshotrs41564222
SNPdbers41564222
MSV3drs41564222
GWAS Ctlgrs41564222
Max Magnitude0
ClinVar
Risk rs41564222(G,T;G,T)
Alt rs41564222(G,T;G,T)
Reference rs41564222(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324677G>A; NC_000006.11:g.31324677G>C
CLNSRC
CLNACC