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rs41561613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41561613(A;A)
Make rs41561613(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356850
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41561613
ebirs41561613
HLIrs41561613
Exacrs41561613
Varsomers41561613
Maprs41561613
PheGenIrs41561613
hapmaprs41561613
1000 genomesrs41561613
hgdprs41561613
ensemblrs41561613
gopubmedrs41561613
geneviewrs41561613
scholarrs41561613
googlers41561613
pharmgkbrs41561613
gwascentralrs41561613
openSNPrs41561613
23andMers41561613
23andMe allrs41561613
SNP Nexus

SNPshotrs41561613
SNPdbers41561613
MSV3drs41561613
GWAS Ctlgrs41561613
Max Magnitude0
ClinVar
Risk rs41561613(A,C,T;A,C,T)
Alt rs41561613(A,C,T;A,C,T)
Reference rs41561613(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324627C>A; NC_000006.11:g.31324627C>G; NC_000006.11:g.31324627C>T
CLNSRC
CLNACC