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rs41544412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41544412(A;G)
Make rs41544412(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355435
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41544412
ebirs41544412
HLIrs41544412
Exacrs41544412
Varsomers41544412
Maprs41544412
PheGenIrs41544412
hapmaprs41544412
1000 genomesrs41544412
hgdprs41544412
ensemblrs41544412
gopubmedrs41544412
geneviewrs41544412
scholarrs41544412
googlers41544412
pharmgkbrs41544412
gwascentralrs41544412
openSNPrs41544412
23andMers41544412
23andMe allrs41544412
SNP Nexus

SNPshotrs41544412
SNPdbers41544412
MSV3drs41544412
GWAS Ctlgrs41544412
Max Magnitude0
ClinVar
Risk rs41544412(G;G)
Alt rs41544412(G;G)
Reference rs41544412(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323212T>C
CLNSRC
CLNACC