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rs41548215

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41548215(A;G)
Make rs41548215(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355128
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548215
ebirs41548215
HLIrs41548215
Exacrs41548215
Varsomers41548215
Maprs41548215
PheGenIrs41548215
hapmaprs41548215
1000 genomesrs41548215
hgdprs41548215
ensemblrs41548215
gopubmedrs41548215
geneviewrs41548215
scholarrs41548215
googlers41548215
pharmgkbrs41548215
gwascentralrs41548215
openSNPrs41548215
23andMers41548215
23andMe allrs41548215
SNP Nexus

SNPshotrs41548215
SNPdbers41548215
MSV3drs41548215
GWAS Ctlgrs41548215
GMAF0.002296
Max Magnitude0
ClinVar
Risk rs41548215(G;G)
Alt rs41548215(G;G)
Reference rs41548215(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322905T>C
CLNSRC
CLNACC