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rs41562214

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562214(A;A)
Make rs41562214(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356170
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562214
ebirs41562214
HLIrs41562214
Exacrs41562214
Varsomers41562214
Maprs41562214
PheGenIrs41562214
hapmaprs41562214
1000 genomesrs41562214
hgdprs41562214
ensemblrs41562214
gopubmedrs41562214
geneviewrs41562214
scholarrs41562214
googlers41562214
pharmgkbrs41562214
gwascentralrs41562214
openSNPrs41562214
23andMers41562214
23andMe allrs41562214
SNP Nexus

SNPshotrs41562214
SNPdbers41562214
MSV3drs41562214
GWAS Ctlgrs41562214
Max Magnitude0
ClinVar
Risk rs41562214(A,T;A,T)
Alt rs41562214(A,T;A,T)
Reference rs41562214(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323947C>A; NC_000006.11:g.31323947C>T
CLNSRC
CLNACC