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rs41549912

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41549912(C;C)
Make rs41549912(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356780
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41549912
ebirs41549912
HLIrs41549912
Exacrs41549912
Varsomers41549912
Maprs41549912
PheGenIrs41549912
hapmaprs41549912
1000 genomesrs41549912
hgdprs41549912
ensemblrs41549912
gopubmedrs41549912
geneviewrs41549912
scholarrs41549912
googlers41549912
pharmgkbrs41549912
gwascentralrs41549912
openSNPrs41549912
23andMers41549912
23andMe allrs41549912
SNP Nexus

SNPshotrs41549912
SNPdbers41549912
MSV3drs41549912
GWAS Ctlgrs41549912
Max Magnitude0
ClinVar
Risk rs41549912(A,C;A,C)
Alt rs41549912(A,C;A,C)
Reference rs41549912(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324557C>G; NC_000006.11:g.31324557C>T
CLNSRC
CLNACC