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rs41560213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560213(A;A)
Make rs41560213(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356912
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560213
ebirs41560213
HLIrs41560213
Exacrs41560213
Varsomers41560213
Maprs41560213
PheGenIrs41560213
hapmaprs41560213
1000 genomesrs41560213
hgdprs41560213
ensemblrs41560213
gopubmedrs41560213
geneviewrs41560213
scholarrs41560213
googlers41560213
pharmgkbrs41560213
gwascentralrs41560213
openSNPrs41560213
23andMers41560213
23andMe allrs41560213
SNP Nexus

SNPshotrs41560213
SNPdbers41560213
MSV3drs41560213
GWAS Ctlgrs41560213
Max Magnitude0
ClinVar
Risk rs41560213(A,C,T;A,C,T)
Alt rs41560213(A,C,T;A,C,T)
Reference rs41560213(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324689C>A; NC_000006.11:g.31324689C>G; NC_000006.11:g.31324689C>T
CLNSRC
CLNACC