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rs41552212

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41552212(A;G)
Make rs41552212(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356738
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552212
ebirs41552212
HLIrs41552212
Exacrs41552212
Varsomers41552212
Maprs41552212
PheGenIrs41552212
hapmaprs41552212
1000 genomesrs41552212
hgdprs41552212
ensemblrs41552212
gopubmedrs41552212
geneviewrs41552212
scholarrs41552212
googlers41552212
pharmgkbrs41552212
gwascentralrs41552212
openSNPrs41552212
23andMers41552212
23andMe allrs41552212
SNP Nexus

SNPshotrs41552212
SNPdbers41552212
MSV3drs41552212
GWAS Ctlgrs41552212
Max Magnitude0
ClinVar
Risk rs41552212(G,T;G,T)
Alt rs41552212(G,T;G,T)
Reference rs41552212(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324515T>A; NC_000006.11:g.31324515T>C
CLNSRC
CLNACC