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rs41541222

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41541222(G;T)
Make rs41541222(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942926
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41541222
ebirs41541222
HLIrs41541222
Exacrs41541222
Varsomers41541222
Maprs41541222
PheGenIrs41541222
hapmaprs41541222
1000 genomesrs41541222
hgdprs41541222
ensemblrs41541222
gopubmedrs41541222
geneviewrs41541222
scholarrs41541222
googlers41541222
pharmgkbrs41541222
gwascentralrs41541222
openSNPrs41541222
23andMers41541222
23andMe allrs41541222
SNP Nexus

SNPshotrs41541222
SNPdbers41541222
MSV3drs41541222
GWAS Ctlgrs41541222
GMAF0.1074
Max Magnitude0
ClinVar
Risk rs41541222(A,C,T;A,C,T)
Alt rs41541222(A,C,T;A,C,T)
Reference rs41541222(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910703G>A; NC_000006.11:g.29910703G>C; NC_000006.11:g.29910703G>T
CLNSRC
CLNACC