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rs41563412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563412(A;A)
Make rs41563412(A;G)
Make rs41563412(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356966
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563412
ebirs41563412
HLIrs41563412
Exacrs41563412
Varsomers41563412
Maprs41563412
PheGenIrs41563412
hapmaprs41563412
1000 genomesrs41563412
hgdprs41563412
ensemblrs41563412
gopubmedrs41563412
geneviewrs41563412
scholarrs41563412
googlers41563412
pharmgkbrs41563412
gwascentralrs41563412
openSNPrs41563412
23andMers41563412
23andMe allrs41563412
SNP Nexus

SNPshotrs41563412
SNPdbers41563412
MSV3drs41563412
GWAS Ctlgrs41563412
Max Magnitude0
ClinVar
Risk rs41563412(A,G,T;A,G,T)
Alt rs41563412(A,G,T;A,G,T)
Reference rs41563412(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324743G>A; NC_000006.11:g.31324743G>C
CLNSRC
CLNACC