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rs41548819

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41548819(A;A)
Make rs41548819(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356390
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548819
ebirs41548819
HLIrs41548819
Exacrs41548819
Varsomers41548819
Maprs41548819
PheGenIrs41548819
hapmaprs41548819
1000 genomesrs41548819
hgdprs41548819
ensemblrs41548819
gopubmedrs41548819
geneviewrs41548819
scholarrs41548819
googlers41548819
pharmgkbrs41548819
gwascentralrs41548819
openSNPrs41548819
23andMers41548819
23andMe allrs41548819
SNP Nexus

SNPshotrs41548819
SNPdbers41548819
MSV3drs41548819
GWAS Ctlgrs41548819
Max Magnitude0
ClinVar
Risk rs41548819(A,T;A,T)
Alt rs41548819(A,T;A,T)
Reference rs41548819(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324167G>A; NC_000006.11:g.31324167G>T
CLNSRC
CLNACC