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rs41544912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41544912(G;T)
Make rs41544912(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356391
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41544912
ebirs41544912
HLIrs41544912
Exacrs41544912
Varsomers41544912
Maprs41544912
PheGenIrs41544912
hapmaprs41544912
1000 genomesrs41544912
hgdprs41544912
ensemblrs41544912
gopubmedrs41544912
geneviewrs41544912
scholarrs41544912
googlers41544912
pharmgkbrs41544912
gwascentralrs41544912
openSNPrs41544912
23andMers41544912
23andMe allrs41544912
SNP Nexus

SNPshotrs41544912
SNPdbers41544912
MSV3drs41544912
GWAS Ctlgrs41544912
Max Magnitude0
ClinVar
Risk rs41544912(A,C,T;A,C,T)
Alt rs41544912(A,C,T;A,C,T)
Reference rs41544912(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324168C>A; NC_000006.11:g.31324168C>G; NC_000006.11:g.31324168C>T
CLNSRC
CLNACC